Who is the manufacturer of MIS Angulated multi-unit abutments?

Dentsply Sirona filed the 510(k) submission for MIS Angulated multi-unit abutments (K213432).

What is the FDA product code for MIS Angulated multi-unit abutments?

NHA. It is classified under 21 CFR 872.3630 as a Class 2 device in the Dental panel.

What is the regulatory pathway for MIS Angulated multi-unit abutments?

510(k) clearance (submission type: Traditional).

What are the predicate devices for MIS Angulated multi-unit abutments?

MIS V3 Conical Connection Dental Implant System (K163349).

Who can help prepare an FDA 510(k) submission like MIS Angulated multi-unit abutments?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

MIS Angulated multi-unit abutments

K213432 · Dentsply Sirona · NHA · Apr 1, 2022 · Dental

Device Facts

Record ID	K213432
Device Name	MIS Angulated multi-unit abutments
Applicant	Dentsply Sirona
Product Code	NHA · Dental
Decision Date	Apr 1, 2022
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 872.3630
Device Class	Class 2
Attributes	Therapeutic

Intended Use

MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.30mm) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for prosthetic devices such as artificial teeth. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. The long MIS (18 & 20mm) implants can be used in a tilted manner. MIS short implants are to be used only with straight abutments. M4 short implants are indicated for delayed loading only.

Device Story

MIS Angulated multi-unit abutments are endosseous dental implant components used to anchor screw-retained multiple-unit restorations. The system includes a one-piece abutment, a prosthetic multi-unit screw, and a titanium gripping bar for positioning. The device connects to MIS dental implants via conical or internal-hex connections. The cementing cap serves as a superstructure interface for permanent restorations. Used in dental clinics by trained professionals, the device provides a stable foundation for prosthetic teeth. By allowing for angulated placement (17° or 30°), the system enables clinicians to compensate for implant trajectory, facilitating optimal prosthetic alignment in patients with varying bone anatomy. This improves the feasibility of fixed restorations in complex cases, ultimately restoring masticatory function and aesthetics for the patient.

Clinical Evidence

No clinical data was included. Substantial equivalence is supported by bench testing, specifically dynamic fatigue testing per ISO 14801:2016, demonstrating the device withstands 5,000,000 cycles without failure. Sterilization validation (gamma irradiation for sterile components, moist heat for non-sterile components) and shelf-life testing (5-year claim) were also provided.

Technological Characteristics

Materials: Titanium (ASTM F136-13). Design: One-piece abutment with multi-unit screw; 17° and 30° angulations; Narrow, Standard, and Wide platforms. Connection: Conical or Internal-hex. Sterilization: Gamma irradiation (sterile components) or moist heat (non-sterile components). Connectivity: None (mechanical device).

Indications for Use

Indicated for surgical placement in upper or lower jaw bone to support prosthetic devices (artificial teeth) for masticatory function restoration. Narrow implants (Ø3.30mm) restricted to mandibular central/lateral incisors and maxillary lateral incisors in partially edentulous patients; requires splinting for adjacent narrow implants. Contraindicated for immediate loading of M4 short implants (delayed loading only) and use of short implants with angulated abutments.

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

MIS V3 Conical Connection Dental Implant System (K163349)

Reference Devices

MIS C1 Wide Platform Conical Connection Abutment (K172505)
MIS Internal Hex Dental Implant System (K180282)
Ankylos Balance Base Abutments (K122268)

Related Devices

K101798 — SPI VARIOMULTI ANGLED ABUTMENT · Thommen Medical AG · Aug 19, 2010
K203252 — Multi-unit Abutments for CONELOG · BioHorizons Implant Systems, Inc. · Mar 16, 2021
K191123 — Multi-unit Abutments · Medentika GmbH · Jan 6, 2020
K121688 — MULTI-UNIT ABUTMENTS WITH ANGULATIONS 17 AND 30 FOR TAPERED IMPLANT SYSTEM · Prismatik Dentalcraft, Inc. · Oct 12, 2012
K081851 — NEOSS ACCESS ABUTMENTS · Neoss, Ltd. · Mar 2, 2009

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logos of the Department of Health and Human Services and the Food and Drug Administration (FDA). The Department of Health and Human Services logo is on the left, and the FDA logo is on the right. The FDA logo includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text. Dentsply Sirona Courtney Clark Sr. Director of Regulatory Affairs 221 West Philadelphia Street, Suite 60W York, Pennsylvania 17401 ### Re: K213432 Trade/Device Name: MIS Angulated multi-unit abutments Regulation Number: 21 CFR 872.3630 Regulation Name: Endosseous Dental Implant Abutment Regulatory Class: Class II Product Code: NHA Dated: March 3, 2022 Received: March 4, 2022 #### Dear Courtney Clark: 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 (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 located 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}------------------------------------------------ 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 803) for devices or postmarketing safety reporting (21 CFR 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 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 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. 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 Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) #### K213432 Device Name MIS Angulated multi-unit abutments #### Indications for Use (Describe) MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.30mm) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for prosthetic devices such as artificial teeth. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. The long MIS (18 & 20mm) implants can be used in a tilted manner. MIS short implants are to be used only with straight abutments. M4 short implants are indicated for delayed loading only. | 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." {3}------------------------------------------------ Dentsply Sirona 221 West Philadelphia Street Suite 60W York, PA 17401 Image /page/3/Picture/1 description: The image shows the logo for Dentsply Sirona. The logo consists of a stylized, abstract shape on the left, resembling a curved leaf or a stylized "S". To the right of the shape are the words "Dentsply" stacked on top of "Sirona". The logo is simple and modern, with a focus on the company's name. ### 510(k) SUMMARY for MIS Angulated multi-unit abutments - K213432 #### 1. Submitter Information: Dentsply Sirona 221 West Philadelphia Street Suite 60W York, PA 17401 Primary Contact Person: Courtney Clark Telephone Number: 248-895-4379 Fax Number: 717-849-4343 Date Prepared: April 1, 2022 # 2. Device Name: . - Proprietary Name: ● MIS Angulated multi-unit abutments - Classification Name: ● Endosseous dental implant abutment - CFR Number: 872.3630 - Device Class: II - Product Code: . NHA - 3. Predicate Device: The primary predicate and reference devices identified relating to the substantial equivalence for the MIS Angulated multi-unit abutments are: | Primary Predicate Device Name | 510(k) | Company Name | |-----------------------------------------------------|---------|-----------------------------------------------------| | MIS V3 Conical Connection Dental Implant System | K163349 | MIS Implants Technologies Ltd. (Dentsply Sirona) | | Reference Device Name | 510(k) | Company Name | | MIS C1 Wide Platform Conical Connection Abutment | K172505 | MIS Implants Technologies Ltd. (Dentsply Sirona) | | MIS Internal Hex Dental Implant System | K180282 | MIS Implants Technologies Ltd. (Dentsply Sirona) | | Ankylos Balance Base Abutments | K122268 | Dentsply Sirona Implants (Dentsply Sirona) | {4}------------------------------------------------ # 4. Description of Device: The proposed MIS Angulated multi-unit abutments are endosseous dental implant abutments that are connected to MIS dental implants and used as an aid in prosthetic rehabilitation, for anchoring screw retained multiple-unit restorations. MIS Angulated multi-unit abutments consist of a one-piece abutment and a prosthetic multi-unit screw, both made of Titanium complying with ASTM F136-13 (Standard Specification for Wrought Titanium-6 Aluminum-4 Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications (USN R56401). The proposed abutments are available in 17° and 30° angulations and connected to the implant by a prosthetic multi-unit screw supplied with the proposed abutments. The proposed abutments are also supplied with a titanium gripping bar used to position the multi-unit abutment on the implant. The proposed abutments are supplied sterile to the user. Table 4.1 below summarizes the main specifications of the proposed MIS Angulated multi-unit abutments and the modifications made. | Element | Specifications | Modifications/Changes | |--------------------------------------------|--------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------| | Connection | -Conical (C1, V3) -Internal-hex Connection (SEVEN, Lance +, M4) | Same connections Proposed abutments are compatible with multiple conical and internal-hex connections | | Platform | -Narrow Platform (NP) -Standard Platform (SP) -Wide Platform (WP) | New NP for angulated multi-unit abutments | | Implant platform diameter | -NP: Ø3.3 mm -SP: Ø 3.75, 3.9, 4.2, 4.3, 5.0 mm -WP: Ø 5.0, 6.0 mm | New NP Other platform diameters remain the same. | | Gingival height | -1 and 2 mm for NP -3 mm for SP and WP | New gingival height of 3 mm for SP and WP | | Angulations | 17° and 30° for all platforms | Same angulations | | Prosthetic screw Implant to abutment | -Multi-unit screw for SP and WP: MU-SOP01A (cleared in K163349) -Screw for NP: New, MU-SOPN1A | Same materials and same screw for SP and WP. New multi-unit screw to fit the NP abutments | Table 4.1: Specifications of the Proposed MIS Angulated multi-unit abutments The proposed MIS cementing cap is a superstructure that has a standard connection design intended to be directly connected to all MIS straight and angulated multi-unit abutments with a prosthetic screw. The proposed cementing cap and prosthetic screw are made of Titanium complying with ASTM F136-13. Multi-unit cementing caps are delivered non-sterile, and are intended to be cleaned and steamsterilized by a professional user according to the instructions before use. # 5. Indications for Use: MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (03.30mm) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to {5}------------------------------------------------ provide support for prosthetic devices such as artificial teeth. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. The long MIS (18 & 20mm) implants can be used in a tilted manner. MIS short implants are to be used only with straight abutments. M4 short implants are indicated for delayed loading only. # 6. Substantial Equivalence: The design of the proposed MIS Angulated multi-unit abutments is based on the design of angulated multi-unit abutments cleared under primary predicate (K163349) and reference devices (K172505, K180282). The abutment diameter, implant-abutment-superstructure connection, and angulations are identical. The proposed MIS Angulated multi-unit abutments include a higher gingival height for Standard and Wide Platforms and are also available in a Narrow Platform. An overview of the similarities and differences between the proposed and the primary predicate device (K163349) is given in Table 6.1. below. A discussion of the similarities and differences follows Table 6.1. {6}------------------------------------------------ # Table 6.1: Comparison between the proposed MIS Angulated multi-unit abutments and primary predicate device and reference devices | Element | Proposed devices MIS angulated multi-unit abutments and cementing cap | Primary predicate MIS V3 conical connection angulated multi-unit abutments and superstructure (K163349) | Reference device MIS Internal Hex angulated multi-unit abutment (K180282) | Reference device MIS C1 conical connection angulated multi-unit abutment (K172505) | Reference device Ankylos Balance Base angulated multi-unit abutment (K122268) | |------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Indications for Use | MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.30mm) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for prosthetic devices such as artificial teeth. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. The long MIS (18 & 20mm) implants can be used in a tilted manner. MIS short implants are to be used only with straight abutments. M4 short implants are indicated for delayed loading only. | MIS V3 Conical Connection Dental Implant System is intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.3mm) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for prosthetic devices such as artificial teeth, in order to restore the patient chewing function. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. | MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.30mm & UNO) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for prosthetic devices such as artificial teeth. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. The long MIS (18 & 20mm) implants can be used in a tilted manner. MIS short implants are to be used only with straight abutments. M4 short implants are indicated for delayed loading only. | MIS dental implant system is intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.3mm & UNO) are indicated for use in surgical and restorative applications for placement only in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for prosthetic devices such as artificial teeth, in order to restore the patient chewing function. Mandibular central and lateral incisors must be splinted if using two or more narrow implants adjacent to one another. | The angled ANKYLOS® Balance Base Abutments are indicated for use in prosthetic restorations with Ankylos® implants and bridges or bar overdentures using a minimum of 2 implants. In edentulous jaws, immediate loading is possible using a minimum of 4 implants. Implants may be tilted up to 45°. When used with angulations between 30° and 45° in edentulous arch, a minimum of four implants must be used and splinted. | | Manufacturer | MIS Implants Technologies Ltd. (Dentsply Sirona) | MIS Implants Technologies Ltd. (Dentsply Sirona) | MIS Implants Technologies Ltd. (Dentsply Sirona) | MIS Implants Technologies Ltd. (Dentsply Sirona) | Dentsply Sirona | | Device Class | Class II | Class II | Class II | Class II | Class II | | Product code(s) | NHA, Endosseous dental implant abutment | NHA, Endosseous dental implant abutment | NHA, Endosseous dental implant abutment | NHA, Endosseous dental implant abutment | NHA, Endosseous dental implant abutment | | Element | Proposed devices MIS angulated multi-unit abutments and cementing cap | Primary predicate MIS V3 conical connection angulated multi-unit abutments and superstructure (K163349) | Reference device MIS Internal Hex angulated multi-unit abutment (K180282) | Reference device MIS C1 conical connection angulated multi-unit abutment (K172505) | Reference device Ankylos Balance Base angulated multi-unit abutment (K122268) | | Material | Titanium | Titanium | Titanium | Titanium | Titanium | | Surface treatment | Polished and anodized / Only polished | Polished and anodized after machined | Polished after machined | Polished and anodized after machined | Polished after machined | | Screw connection | One abutment screw for connection of the multi-unit to the implant. Prosthetic screw for connection of the superstructure (cementing cap) to the multi-unit | One abutment screw for connection of the multi- unit to the implant. Prosthetic screw for connection of the temporary superstructure to the multi-unit | One abutment screw for connection of the multi- unit to the implant. Prosthetic screw for connection of the temporary superstructure to the multi-unit | One abutment screw for connection of the multi- unit to the implant. Prosthetic screw for connection of the temporary superstructure to the multi-unit | Abutment screw for connection to the implant. 2-piece abutment, abutment head screws into main abutment body. Prosthetic screw for connection to the abutment | | Abutment- superstructure interface | Screw secured, with a plate to plate sealing surface | Screw secured, with a plate to plate sealing surface | Screw secured, with a plate to plate sealing surface | Screw secured, with a plate to plate sealing surface | Screw secured, with a plate to plate sealing surface | | Restoration | Multiple-units | Multiple-units | Multiple-units | Multiple-units | Multiple-units | | Restoration type | Screw-retained | Screw-retained | Screw-retained | Screw-retained | Screw-retained | | Abutment diameter | Ø 4.80 | Ø 4.80 | Ø 4.80 | Ø 4.80 | Ø 4.20 | | Implant to abutment connection | -MIS C1 Conical Connection -MIS V3 Conical Connection -MIS SEVEN Internal Hex -MIS M4 Internal Hex -MIS Lance+ Internal Hex | MIS V3 Conical Connection…