TiGEN Abutment, PMMA Abutment and Scan Healing Abutment

K234142 · Megagen Implant Co., Ltd. · NHA · Sep 18, 2024 · Dental

Device Facts

Record IDK234142
Device NameTiGEN Abutment, PMMA Abutment and Scan Healing Abutment
ApplicantMegagen Implant Co., Ltd.
Product CodeNHA · Dental
Decision DateSep 18, 2024
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 872.3630
Device ClassClass 2
AttributesTherapeutic

Intended Use

The TiGEN Abutment, PMMA Abutment and Scan Healing Abutment are intended for use on endosseous dental implants in the edentulous or partially edentulous maxilla or mandible, as an aid in prosthetic rehabilitation. The PMMA Abutment is indicated to be used prior to the final components to maintain, stabilize and shape the soft tissue during the healing phase. They must be placed out of occlusion and are for temporary use (3 months). For TiGEN Abutment and PMMA Abutment, all digitally designed abutments for use with PMMA Abutment and TiGEN Abutment are intended to be sent to a MegaGen-validated milling center for manufacture.

Device Story

System comprises TiGEN Abutment, PMMA Abutment, and Scan Healing Abutment for endosseous dental implants. TiGEN Abutment (Ti-6Al-4V ELI) is a patient-specific, CAD/CAM-machined abutment for final prosthetic support. PMMA Abutment (PMMA post, Ti-6Al-4V ELI cuff) is a temporary component for soft tissue healing (up to 3 months). Scan Healing Abutment is a scannable component for soft tissue contouring and digital impression capture. Devices are used in dental clinics by clinicians. CAD/CAM designs for TiGEN and PMMA abutments are transmitted to MegaGen-validated milling centers for fabrication. Output is a custom abutment or temporary healing component. Benefits include patient-specific prosthetic fit, soft tissue management, and streamlined digital workflow. Devices are MR Conditional.

Clinical Evidence

Bench testing only. Performance evaluated via fatigue testing per ISO 14801. Biocompatibility assessed per ISO 10993-1. Sterilization validated per ISO 17665-2 (steam) and ISO 11137 (gamma). Shelf life validated to 5 years per ASTM F1980-07. MR compatibility assessed via reference to K230618.

Technological Characteristics

Materials: Ti-6Al-4V ELI alloy, PMMA. Sensing/Actuation: CAD/CAM patient-specific design. Connectivity: Digital design files sent to validated milling centers. Sterilization: Non-sterile (user steam sterilization) for TiGEN/PMMA; Gamma-sterile for Scan Healing Abutment. Form factor: Custom-milled abutments and healing components. Standards: ISO 14801 (fatigue), ISO 10993-1 (biocompatibility), ASTM F1980 (shelf life).

Indications for Use

Indicated for use on endosseous dental implants in edentulous or partially edentulous maxilla or mandible for prosthetic rehabilitation. PMMA Abutment indicated for temporary (3 months) soft tissue maintenance, stabilization, and shaping prior to final restoration; must be placed out of occlusion.

Regulatory Classification

Identification

An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation.

Special Controls

*Classification.* Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Root-Form Endosseous Dental Implants and Endosseous Dental Implant Abutments” will serve as the special control. (See § 872.1(e) for the availability of this guidance document.)

Predicate Devices

Reference Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, with the letters "FDA" in a blue square. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. MegaGen Implant Co., Ltd. Hyo-Eun Lee Official Correspondent 45, Secheon-ro 7-gil, Dasa-eup, Dalseong-gun Daegu, 42921 REPUBLIC OF KOREA September 18, 2024 # Re: K234142 Trade/Device Name: TiGEN Abutment: PMMA Abutment and Scan Healing Abutment Regulation Number: 21 CFR 872.3630 Regulation Name: Endosseous dental implant abutment Regulatory Class: Class II Product Code: NHA Dated: September 11, 2024 Received: September 13, 2024 Dear Hyo-Eun Lee: We have reviewed your section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (the Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. {1}------------------------------------------------ Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download). Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30. Design controls; 21 CFR 820.90. Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181). Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050. All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-device-advicecomprehensive-regulatory-assistance/unique-device-identification-system-udi-system. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems. {2}------------------------------------------------ 3 For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, # Andrew I. Steen -S Andrew I. Steen Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT, and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ # Indications for Use 510(k) Number (if known) K234142 Device Name TiGEN Abutment, PMMA Abutment and Scan Healing Abutment Indications for Use (Describe) The TiGEN Abutment, PMMA Abutment and Scan Healing Abutment are intended for use on endosseous dental implants in the edentulous or partially edentulous maxilla or mandible, as an aid in prosthetic rehabilitation. The PMMA Abutment is indicated to be used pror to the final components to maintain, stabilize and shape the soft tissue during the healing plase. They must be placed out of occlusion and are for temporary use (3 months). For TiGEN Abutment and PMMA Abutment, all digitally designed abutments for use with PMMA Abutment and TiGEN Abutment are intended to be sent to a MegaGen-validated milling center for manufacture. | Type of Use (Select one or both, as applicable) | | |-------------------------------------------------|--| |-------------------------------------------------|--| X | Prescription Use (Part 21 CFR 801 Subpart D) | Over-The-Counter Use (21 CFR 801 Subpart C) # CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. # *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {4}------------------------------------------------ ## 510(k) Summary This 510(k) Summary is being submitted in accordance with the requirements of 21 CFR Part 807.92. ## K234142 Spetember 17, 2024 ## 1. Applicant / Submitter MegaGen Implant Co., Ltd. 45, Secheon-ro, 7-gil, Dasa-eup, Dalseong-gun, Daegu, Republic of Korea Tel: + 82-53-222-2828 ## 2. Submission Correspondent Hyo-Eun, Lee MegaGen Implant Co., Ltd. 45, Secheon-ro, 7-gil, Dasa-eup, Dalseong-gun, Daegu, Republic of Korea Tel: +82-53-222-3860 Fax: +82-53-289-3414 Email: ra7@imegagen.com ## 3. Device | • Trade Name: | TiGEN Abutment, PMMA Abutment and Scan Healing Abutment | |----------------|---------------------------------------------------------| | • Common Name: | Endosseous Dental Implant Abutment | - Endosseous Dental Implant Abutment Classification Name: - NHA • Primary Product Code: - Class II, 21 CFR 872.3630 • Classification regulation: #### Predicate Device 4. • ## • Primary Predicate Device: K220562 - TiGEN Abutment, ZrGEN Abutment and Scan Healing Abutment ## • Reference Device: K150203 – Medentika CAD/CAN Abutments K220751 – Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA K122192 - Straumann Temporary Abutments VITA CAD-Temp K203554 - AnyOne External Implant System K210161 - AnyOne Onestage Implant System K230618 - MegaGen Dental Implant Systems Portfolio - MR Conditional K233208 - NobelProcera® Titanium ASC Abutment, Omnigrip Clinical Screw Titanium {5}------------------------------------------------ #### 5. Description #### . TiGEN Abutment The TiGEN Abutment is machined with the final prosthetic in accordance with the intraoral structure. It is machined by using dental CAD/CAM technology in accordance with customized patient's information in MegaGen-validated milling center. The TiGEN Abutment is made of Ti-6Al-4V ELI alloy. And It is provided with abutment screw. All TiGEN Abutment is provided non-sterile. The milled TiGEN Abutment must be sterilized by users prior to use. | System | Type | Minimum<br>wall<br>thickness<br>(mm) | Maximum<br>angulation<br>(°) | Minimum<br>gingival<br>collar<br>height<br>(mm) | Maximum<br>gingival<br>collar<br>height<br>(mm) | Minimum<br>gingival<br>collar<br>(ø) | Maximum<br>gingival<br>collar<br>(ø) | Minimum<br>post height<br>(mm) | Maximum<br>post height<br>(mm) | |--------|------------------|--------------------------------------|------------------------------|-------------------------------------------------|-------------------------------------------------|--------------------------------------|--------------------------------------|--------------------------------|--------------------------------| | AR | Holder | 0.67 | | | 5 | 4 | | | | | AO | Holder | 0.7 | | | 5 | 4.5 | | | | | MN | Holder | 0.5 | | | 5 | 3.5 | | | | | BD | Holder | 0.71 | 30 | 2 | 5 | 4 | 11.5 | 4 | 6 | | | Holder<br>Bridge | 0.46 | | | 5 | 4 | | | | | AOO | Holder | 0.05 | | | 3 | 4.8 | | | | | AOE | Holder | 0.3 | | | 5 | 4 | | | | The allowable ranges of design parameters after CAD/CAM patient-matching are follows: The post height is defined as the cementable height of the abutment. | | The TiGEN Abutment is compatible with following MEGAGEN Implants and Screw cleared under: | | | | | |--|-------------------------------------------------------------------------------------------|--|--|--|--| |--|-------------------------------------------------------------------------------------------|--|--|--|--| | Compatibility Fixture | | | Compatibility Screw | | | |----------------------------------------|---------------------------------|---------------------------|--------------------------------------------------|----------------------------------|------------------------------------| | Compatible Implant System | Product Name | 510(k) Number | The widest Diameter (mm) | Product Name | 510(k) Number | | Xpeed AnyRidge Internal Implant System | Xpeed AnyRidge Internal Fixture | K122231, K123870, K140091 | 4.0, 4.4, 4.9, 5.4, 5.9, 6.4, 6.9, 7.4, 7.9, 8.4 | Multi Post Screw | K122231, K123870, K140091, K110955 | | AnyOne Internal Implant System | AnyOne Internal Fixture | K123988 | 3.9, 4.3, 4.8, 5.3, 5.8, 6.3, 6.8, 7.3, 7.8, 8.3 | Abutment Screw | K182448 | | BLUEDIAMOND IMPLANT System | BLUEDIAMOND IMPLANT | K182448 | 3.6, 3.7, 4.0, 4.1, 4.4, 4.8, 5.0, 5.5 | Abutment Screw | K123988 | | AnyOne External Implant System | AnyOne External Fixture | K052369, K203554 | 3.9, 4.3, 4.8, 5.3, 5.8, 6.3, 6.8 | Abutment Screw | K052369, K203554 | | AnyOn Onestage Implant System | AnyOn Onestage Fixture | K210161 | 3.9, 4.3, 4.8, 5.3 | Multi Post Screw, Abutment Screw | K210161 | | MINI Internal Implant System | MINI Internal Fixture | K150537 | 3.0, 3.4 | Abutment Screw | K150537 | [Note] There is the modification of the Implant System Name for FDA cleared AnyRidge Octa 1 Implant System to BLUEDIAMOND IMPLANT System with K182448. According to below FDA Guidance*, MEGAGEN manages it as a 510(k) VARIANCE REQIEST FORM for changes. *Deciding When to Submit a 510(k) for a Change to an Existing Device / Guidance for Industry and Food and Drug Administration Staff / Document issued on October 25, 2017. #### . PMMA Abutment The PMMA Abutment is a temporary prosthesis used until the final prosthesis is placed for up to three months. The PMMA Post is machined with the temporary prosthetic in accordance with the intraoral structure by using dental CAD/CAM technology. The PMMA Cuff is made of Ti-6Al-4V ELI alloy and available in various gingival heights. The PMMA Post is made of Polymethyl methacrylate and available in various diameters and lengths so that it can be used according to individual patient conditions. All PMMA Abutment is provided non-sterile with abutment screw. The milled PMMA Abutment must be sterilized by users prior to use. {6}------------------------------------------------ | | | Part being milled | | | | | Manufactured part<br>(Not be milled) | | | |--------|---------------------------|------------------------------|-------------------------------------|-------------------------------------|--------------------------------|-----------------------------------|-----------------------------------------|------------------------------|--------------------------------| | System | Wall<br>thickness<br>(mm) | Maximum<br>angulation<br>(°) | Minimum Post<br>diameter<br>(ø, mm) | Maximum Post<br>diameter<br>(ø, mm) | Minimum<br>post height<br>(mm) | Maximum post<br>height<br>(A, mm) | Gingival<br>collar<br>Height<br>(B, mm) | Gingival collar<br>(ø, mm) | Maximum<br>height<br>(A+B, mm) | | AR | | | | | | | | 3.6, 3.7 | | | BD | 0.5 | 30 | 4.5 | 16 | 5.5 | 10.6 | 0.4, 1.3, 2.8 | 3.1, 3.2, 3.4, 3.5, 3.6, 3.7 | 11 | | AO | | | | | | | | 3.5, 3.7 | | The allowable ranges of design parameters after CAD/CAM patient-matching are follows: The PMMA Abutment is compatible with following MEGAGEN Implants and Screw cleared under: | Compatibility Fixture | | | | Compatibility Screw | | |----------------------------------------------|------------------------------------|---------------------------------|-----------------------------------------------------|---------------------|---------------------------------------| | Compatible Implant<br>System | Product Name | 510(k) Number | The widest Diameter<br>(mm) | Product<br>Name | 510(k) Number | | Xpeed AnyRidge<br>Internal Implant<br>System | Xpeed AnyRidge<br>Internal Fixture | K122231,<br>K123870,<br>K140091 | 4.0, 4.4, 4.9, 5.4, 5.9, 6.4,<br>6.9, 7.4, 7.9, 8.4 | Multi Post<br>Screw | K122231, K123870,<br>K140091, K110955 | | AnyOne<br>Internal Implant<br>System | AnyOne<br>Internal Fixture | K123988 | 3.9, 4.3, 4.8, 5.3, 5.8, 6.3,<br>6.8, 7.3, 7.8, 8.3 | Abutment<br>Screw | K182448 | | BLUEDIAMOND<br>IMPLANT System | BLUEDIAMOND<br>IMPLANT | K182448 | 3.6, 3.7, 4.0, 4.1, 4.4, 4.8,<br>5.0, 5.5 | Abutment<br>Screw | K123988 | [Note] There is the modification of the Implant System Name for FDA cleared AnyRidge Octa 1 Implant System to BLUEDIAMOND IMPLANT System with K182448. According to below FDA Guidance*, MEGAGEN manages it as a 510(k) VARIANCE REQIEST FORM for changes. *Deciding When to Submit a 510(k) for a Change to an Existing Device / Guidance for Industry and Food and Drug Administration Staff / Document issued on October 25, 2017. #### . Scan Healing Abutment The Scan Healing Abutment designed to aid in soft tissue contouring during the healing period after implant placement, creating an emergence profile for the final prosthesis. And they have the added design feature to be scannable an intraoral impression by digital scanner. The Scan Healing Abutment is provided with abutment screw and is provided gamma-sterile. The dimensions of scan Healing Abutment are follows: | Device | Component | |-----------------------|-----------------------------------------------------------------------------------------| | Scan Healing Abutment | XPEED AnyRidge Internal Implant System<br>Ø 4.2, 4.7, 5.7, 6.7 x 6.9, 7.9, 9.9, 11.9 mm | | | BLUEDIAMOND IMPLANT System<br>Ø 4.2, 4.7, 5.7, 6.7 x 12.35, 13.85 mm | | | AnyOne Internal Implant System<br>Ø 4.2, 4.7, 5.7, 6.7 x 11.7 mm | The Scan Healing Abutment is compatible with following MEGAGEN Implants and Screw cleared under: | Compatibility Fixture | | | | Compatibility Screw | | |----------------------------------------------|------------------------------------|---------------------------------|-----------------------------------------------------|---------------------|-------------------| | Compatible Implant<br>System | Product Name | 510(k) Number | The widest Diameter (mm) | Product<br>Name | 510(k)<br>Number | | Xpeed AnyRidge<br>Internal Implant<br>System | Xpeed AnyRidge<br>Internal Fixture | K122231,<br>K123870,<br>K140091 | 4.0, 4.4, 4.9, 5.4, 5.9, 6.4,<br>6.9, 7.4, 7.9, 8.4 | | | | AnyOne<br>Internal Implant<br>System | AnyOne<br>Internal Fixture | K123988 | 3.9, 4.3, 4.8, 5.3, 5.8, 6.3,<br>6.8, 7.3, 7.8, 8.3 | S.H.A<br>Screw | Subject<br>Device | | BLUEDIAMOND<br>IMPLANT System | BLUEDIAMOND<br>IMPLANT | K182448 | 3.6, 3.7, 4.0, 4.1, 4.4, 4.8,<br>5.0, 5.5 | | | [Note] There is the modification of the Implant System Name for FDA cleared AnyRidge Octa 1 Implant System to BLUEDIAMOND IMPLANT System with K182448. According to below FDA Guidance*, MEGAGEN manages it as a 510(k) VARIANCE REQIEST FORM for changes. *Deciding When to Submit a 510(k) for a Change to an Existing Device / Guidance for Industry and Food and Drug Administration Staff / Document issued on October 25, 2017. {7}------------------------------------------------ # 6. Indication for use The TiGEN Abutment, PMMA Abutment and Scan Healing Abutment are intended for use on endosseous dental implants in the edentulous or partially edentulous maxilla or mandible, as an aid in prosthetic rehabilitation. The PMMA Abutment is indicated to be used prior to the final components to maintain, stabilize and shape the soft tissue during the healing phase. They must be placed out of occlusion and are for temporary use (3 months). For TiGEN Abutment and PMMA Abutment, all digitally designed abutments for use with PMMA Abutment and TiGEN Abutment are intended to be sent to a MegaGen-validated milling center for manufacture. {8}------------------------------------------------ # 7. Basis for Substantial Equivalence # 7.1. Comparison of the Indications for Use | Table of Substantial Equivalence – Indications for Use | | | | | | |---------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------|-------------------------|--------------------------------|--| | Subject Device<br>(K234142) | Indications for Use | | | | | | MegaGen Co., Ltd. | The TiGEN Abutment, PMMA Abutment and Scan Healing Abutment are intended for use on endosseous dental implants in the edentulous or partially edentulous maxilla or mandible, as an aid in prosthetic rehabilitation. | | | | | | | The PMMA Abutment is indicated to be used prior to the insertion of the final components to maintain, stabilize and shape the soft tissue during the healing phase. They must be placed out of occlusion and are for temporary use (3 months). | | | | | | | For TIGEN Abutment and PMMA Abutment, all digitally designed abutments for use with PMMA Abutment and TiGEN Abutment are intended to be sent to a MegaGen-validated milling center for manufacture. | | | | | | Predicate Device<br>(K220562) | Indications for Use | | | | | | MegaGen Co., Ltd. | The TiGEN Abutment, ZrGEN Abutment and Scan Healing Abutment are intended for use on endosseous dental implants in the edentulous or partially edentulous maxilla or mandible, as an aid in prosthetic rehabilitation. | | | | | | TIGEN Abutment, ZrGEN<br>Abutment and Scan<br>Healing abutment | For TIGEN Abutment and ZrGEN Abutment, all digitally designed abutments for use with TiGEN Abutment and ZrGEN Abutment are intended to be sent to a MegaGen-validated milling center for manufacture. | | | | | | Reference Device | Indications for Use | | | | | | Medentika GmbH | Medentika Preface CAD/CAM Abutments are intended for use with dental implants as a support for single or multiple tooth prostheses in the maxilla or mandible of a partially or fully edentulous patient. | | | | | | MedentikaCAD/CAM<br>Abutments<br>(K150203) | Implant System Compatibility | Series | Implant Diameter (mm) | Platform Diameter (mm) | | | | Nobel Biocare Replace™ Select | E | 3.5, 4.3, 5.0, 6.0 | 3.5, 4.3, 5.0, 6.0 | | | | Nobel Biocare NobelActive™ | F | 3.0, 3.5, 4.3, 5.0 | 3.0, 3.5, 3.9 (4.3), 3.9 (5.0) | | | | Biomet 3i Osseotite® Certain® | H | 3.24, 4.0, 5.0 | 3.4, 4.1, 5.0 | | | | Biomet 3i Osseotite® | I | 3.25, 3.75, 4.0, 5.0 | 3.4, 4.1, 5.0 | | | | Nobel Biocare Brånemark | K | 3.3, 3.75, 4.0, 5.0 | 3.5, 4.1, 4.1, 5.1 | | | | Straumann Bone Level | L | 3.3, 4.1, 4.8 | 3.3, 4.1, 4.8 | | | | Straumann Standard | N | 3.3, 4.1, 4.8 | 3.5(NNC), 4.8, 6.5 | | | | Zimmer Tapered Screw-vent® | R | 3.3, 3.7, 4.1, 4.7, 6.0 | 3.5, 4.5, 5.7 | | | | Astra Tech OsseoSpeed™ | S | 3.0, 3.5, 4.0, 4.5, 5.0 | 3.0, 3.5, 4.0, 4.5, 5.0 | | | | Dentsply Friadent® Frialit/XiVE® | T | 3.4, 3.8, 4.5, 5.5 | 3.4, 3.8, 4.5, 5.5 | | | Institut Straumann AG | Medentika PreFace is intended for use with the Straumann® CARES® System. All digitally designed abutments for use with Medentika CAD/CAM Abutments are intended to be manufactured at a Straumann® CARES® validated milling center. | | | | | | Straumann® BLX Temporary<br>Abutment, VITA CAD-Temp,<br>PMMA<br>(K220751) | Straumann® temporary prosthetic components are indicated to be used prior to the insertion of the final components to maintain, stabilize, and shape the soft tissue during the healing phase. They must not be placed in occlusion. Straumann® temporary abutments are indicated to be placed into Straumann® dental implants to provide a support structure for the functional and esthetic oral rehabilitation of partially edentulous patients with temporary crowns and bridges. | | | | | | Straumann USA, LLC | | | | | | | Straumann Temporary<br>Abutments VITA CAD-<br>Temp<br>(K122192) | Straumann Temporary Abutments VITA CAD-Temp are indicated for use with Straumann Bone Level and Tissue Level implants for temporary crown and bridge restorations, and to maintain, stabilize and shape the soft tissue during the healing phase for up to six months, and should be placed out of occlusion. | | | | | | MegaGen Co., Ltd. | The AnyOne External Implant System is intended to be surgically placed in the maxillary or mandibular | | | | | | AnyOne External Implant<br>System<br>(K203554) | molar areas for the purpose providing prosthetic support for dental restorations (Crown, bridges, and overdentures) in partially or fully edentulous individuals. It is used to restore a patient's chewing function. Smaller implants (less than 6.0 mm) are dedicated for immediate loading when good primary stability is achieved and with appropriate occlusal loading. Larger implants are dedicated for the molar region and are indicated for delayed loading. | | | | | | MegaGen Co., Ltd. | | | | | | | AnyOne Onestage<br>Implant System<br>(K210161) | The AnyOne Onestage Implant System is intended to be surgically placed in the maxillary or mandibular arches for the purpose of providing prosthetic support for dental restorations (Crown, bridges, and overdentures) in partially or fully edentulous individuals. It is used to restore a patient's chewing function in the following situations and with the clinical protocols: -Delayed loading. Immediate loading when good primary stability is achieved and with appropriate occlusal loading. Larger implants are dedicated for the molar region. | | | | | | Substantial Equivalence Discussion | | | | | | {9}------------------------------------------------ The indications for use statement of the same intended use as the primary predicate device, K220562, to support prosthetic rehabilitation when used with dental implants in the maxills or fully edentulous patients. Both the subject device and predicate device are intended for the digitally designed at validated milling centers owned by each applicant. #### 2. Differences The indications for use statement of the subject device is nearly identical to the primary predicate, except for minor changes in wording that do not affect the intended use. Different validated milling centers owned by each applicant are also referenced. For PMMA Abutment are indicated to be used prior to the insertion of the final components to maintain, stabilize and shape the healing phase additionally. This is the same intended use as the reference device, K220751. #### 3. Discussion The differences in the indications for use statement he subject device, primary predicate device(K220751), are only minor changes in wording and do not affect the intended use for demonstrating substantial equivalence. {10}------------------------------------------------ ## 7.2. Comparison for each component ## 7.2.1. TiGEN Abutment | | Subject Device | Predicate Device | Reference Device | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|--|---------| | 510(k) Number | K234142 | K220562 | K150203 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Device Name | TiGEN Abutment | TiGEN Abutment | Medentika CAD/CAM Abutments | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Manufacturer | MegaGen Co., Ltd. | MegaGen Co., Ltd. | Medentika GmbH | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Appearance | Image: TiGEN Abutment | Image: TiGEN Abutment | Unknown | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Material | Ti-6Al-4V ELI | Ti-6Al-4V ELI | Titanium Alloy | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Compatibility | XPEED AnyRidge Internal Implant System<br>BLUEDIAMOND IMPLANT System<br>AnyOne Internal Implant System<br>AnyOne External Implant System<br>AnyOne Onestage Implant System<br>MiNi Internal Implant System | XPEED AnyRidge Internal Implant System<br>BLUEDIAMOND IMPLANT System<br>AnyOne Internal Implant System<br>MiNi Internal Implant System | Unknown | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Implant<br>Diameter<br>(mm) | Xpeed AnyRidge<br>Internal Implant System<br>4.0, 4.4, 4.9, 5.4, 5.9, 6.4,<br>6.9, 7.4, 7.9, 8.4<br>BLUEDIAMOND IMPLANT<br>System<br>3.6, 3.7, 4.0, 4.1, 4.4, 4.8,<br>5.0, 5.5<br>AnyOne<br>Internal Implant System<br>3.9, 4.3, 4.8, 5.3, 5.8, 6.3,<br>6.8, 7.3, 7.8, 8.3<br>AnyOne External Implant<br>System<br>3.9, 4.3, 4.8, 5.3, 5.8, 6.3,<br>6.8<br>AnyOn Onestage Implant<br>System<br>3.9, 4.3, 4.8, 5.3<br>MINi Internal Implant System<br>3.0, 3.4 | Xpeed AnyRidge<br>Internal Implant System<br>4.0, 4.4, 4.9, 5.4, 5.9, 6.4,<br>6.9, 7.4, 7.9, 8.4<br>BLUEDIAMOND IMPLANT<br>System<br>3.6, 3.7, 4.0, 4.1, 4.4, 4.8,<br>5.0, 5.5<br>AnyOne<br>Internal Implant System<br>3.9, 4.3, 4.8, 5.3, 5.8, 6.3,<br>6.8, 7.3, 7.8, 8.3<br>MINi Internal Implant<br>System<br>3.0, 3.4 | Nobel Biocare Replace™ Select E 3.5, 4.3, 5.0, 6.0<br>Nobel Biocare NobelActive™ F 3.0, 3.5, 4.3, 5.0<br>Biomet 3i Osseotite® Certain® H 3.24, 4.0, 5.0<br>Biomet 3i Osseotite® I 3.25, 3.75, 4.0, 5.0<br>Nobel Biocare Brånemark K 3.3, 3.75, 4.0, 5.0<br>Straumann Bone Level L 3.3, 4.1, 4.8<br>Straumann Standard N 3.3, 4.1, 4.8<br>Zimmer Tapered Screw-vent® R 3.3, 3.7, 4.1, 4.7, 6.0<br>Astra Tech OsseoSpeed™ S 3.0, 3.5, 4.0, 4.5, 5.0<br>Dentsply Friadent® Frialit/XiVE® T 3.4, 3.8, 4.5, 5.5 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | CAD/CAM<br>design<br>parameters | System Type Minimum wall thickness (mm) Maximum angulation (°) Minimum gingival collar height (mm) Maximum gingival collar height (mm) Minimum gingival collar (Ø) Maximum gingival collar (Ø) Minimum post height (mm) Maximum post height (mm) AR Holder 0.67 30 2 5 4 4.5 4 6 AO Holder 0.7 MN Holder 0.5 5 4 11.5 6 BD Holder 0.71 AOO Holder 0.05 AOE Holder 0.3 AR: XPEED AnyRidge Internal System<br>AO: AnyOne Internal Implant System<br>MN: MiNi Internal Implant System<br>BD: BLUEDIAMOND IMPLANT System<br>AOO: AnyOne Onestage Implant System<br>AOE: AnyOne External Implant System | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Type Minimum wall thickness (mm) Standard Type 0.47 Maximum angulation (°) 30 Minimum gingival collar height (mm) 2.00 Maximum gingival collar height (mm) 5.00 Minimum gingival collar (Ø) 3.50, 4.00, 4.50 Maximum gingival collar (Ø) 9.50, 11.50 Minimum post height (mm) 4.00 Maximum post height (mm) 6.00, 6.50 Octa level Type Minimum wall thickness (mm) 0.47 Maximum angulation (°) 30 Minimum gingival collar (Ø) 4.00 Maximum gingival collar (Ø) 9.50, 11.50 Minimum post height (mm) 4.00 Maximum post height (mm) 6.00 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Unknown | | Sterilization<br>Method | Non-sterile<br>(Steam sterilized before use) | Non-sterile<br>(Steam sterilized before use) | Non-sterile<br>(Steam sterilized before use) | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Substantial Equivalence Discussion | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | #### 1. Similarities - Material: subject device and predicate device have the same material. - Sterilization Method: Both the subject device are provided as non-sterile and must be sterilized by the user before use. - Diameter: : subject device and predicate device have the same diameter. #### 2.Difference - Compatibility and Implant diameter: For the subject device, TiGEN Abutment of AnyOne Onestage Implant System was added. However, this system has already been to the FDA before with K052369, K203554 and K20161, and the TiGEN Abutment for each system has been tested to confirm the performance. - Total length: Although shorter length is added, it can provide users with a wider range of dimensions. - CAD/CAM design parameters: It has different parameter for each implant system. #### 3. Discussion The subject device and predicate device are used with MegaGen products has already been proven through performance tests. The length of subject device is different. The length may vary depending on the shape of the milling machine. However, safety of subject device was confirmed through the worst-ase when the user manufactures and uses it according to CAD/CAM design parameters, and it can be substantially the same as previously cleared K052369, K203554 and K210161. {11}------------------------------------------------ # 7.2.2. PMMA Abutment | | Subject Device | Predicate Device | Reference Device | | | | |------------------------------------|--------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------|--| | 510(k)<br>Number | K234142 | K220562 | K233208 | K220751 | K122192 | | | Device Name | PMMA Abutment | TIGEN Abutment | NobelProcera<br>Titanium ASC<br>Abutment | Straumann® BLX<br>Temporary<br>Abutment, VITA<br>CAD-Temp,<br>PMMA | Straumann<br>Temporary<br>Abutments VITA<br>CAD-Temp | | | Manufacturer | MegaGen Co., Ltd. | MegaGen Co., Ltd. | Nobel Biocare AB | Institut<br>Straumann AG | Straumann USA,<br>LLC | | | Appearance | Image: PMMA Abutment | Image: TIGEN Abutment…
Innolitics
510(k) Summary
Decision Summary
Classification Order
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