Who is the manufacturer of Tetric CAD?

Ivoclar Vivadent, AG filed the 510(k) submission for Tetric CAD (K173573).

What is the FDA product code for Tetric CAD?

EBF. It is classified under 21 CFR 872.3690 as a Class 2 device in the Dental panel.

What is the regulatory pathway for Tetric CAD?

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

Who can help prepare an FDA 510(k) submission like Tetric CAD?

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.

Tetric CAD

K173573 · Ivoclar Vivadent, AG · EBF · Jun 7, 2018 · Dental

Device Facts

Record ID	K173573
Device Name	Tetric CAD
Applicant	Ivoclar Vivadent, AG
Product Code	EBF · Dental
Decision Date	Jun 7, 2018
Decision	SESE
Submission Type	Abbreviated
Regulation	21 CFR 872.3690
Device Class	Class 2
Attributes	Therapeutic

Intended Use

Tetric® CAD is intended for: - Veneers - Inalys - Onlays (e.g. occlusal veneers, partial crowns) - Crowns in the anterior and posterior region

Device Story

Tetric® CAD is a pre-cured composite block used for chairside fabrication of permanent dental restorations (veneers, inlays, onlays, crowns). The device consists of cross-linked dimethacrylate and inorganic fillers attached to a metal mandrel compatible with CAD/CAM milling systems (e.g., Cerec/InLab, PlanMill, Programill One). The dentist performs intraoral imaging, designs the restoration, and mills the block in a compatible CAD/CAM system. Post-milling, the restoration is polished, characterized, and cemented. The device enables efficient, esthetic, permanent tooth restoration in a single clinical visit. It is intended for professional use by dentists.

Clinical Evidence

Bench testing only. Evaluated physical properties including water solubility (ISO 10477:2004) and flexural strength (ISO 6872:2015) in direct comparison to the predicate. Biocompatibility evaluated per ISO 10993-1:2009, including cytotoxicity (EN ISO 7405:2008, ISO 10993-5:2009) and genotoxicity (ISO 10993-3:2014). Results confirmed the device is non-cytotoxic and non-genotoxic, with physical properties substantially equivalent to the predicate.

Technological Characteristics

Composite block composed of cross-linked dimethacrylate and inorganic fillers. Form factor: blocks with metal mandrel for CAD/CAM milling. Standards: EN 1641:2009 (Dentistry - Medical devices for dentistry - Materials). Flexural strength: 272 MPa. Storage: 2-28°C. Industrially cured; no sterilization required.

Indications for Use

Indicated for patients requiring dental restorations including veneers, inlays, onlays (e.g., occlusal veneers, partial crowns), and crowns in the anterior and posterior regions. Contraindicated for bridge constructions, patients with severely reduced residual dentition, and patients with known allergies to ingredients.

Regulatory Classification

Identification

Tooth shade resin material is a device composed of materials such as bisphenol-A glycidyl methacrylate (Bis-GMA) intended to restore carious lesions or structural defects in teeth.

Predicate Devices

Cerasmart (K133824)

Related Devices

K133824 — CERASMART · GC America, Inc. · Mar 14, 2014
K160425 — CAD/CAMouflage Milling Bock · Prismatik Dentalcraft, Inc. · Jul 15, 2016
K080479 — DENTAL CERAMIC · Dmg USA, Inc. · May 21, 2008
K162537 — CAD/CAMouflage Milling Block · Prismatik Dentalcraft, Inc. · Nov 16, 2016
K153476 — KATANA AVENCIA Block · Kuraray Noritake Dental, Inc. · Aug 23, 2016

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows 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. Ivoclar Vivadent AG % Donna Hartnett Director QA/Regulatory Affairs Ivoclar Vivadent, Inc. 175 Pineview Drive Amherst, New York 14228 Re: K173573 Trade/Device Name: Tetric® CAD Regulation Number: 21 CFR 872.3690 Regulation Name: Tooth Shade Resin Material Regulatory Class: Class II Product Code: EBF Dated: May 3, 2018 Received: May 8, 2018 Dear Donna Hartnett: 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. 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. 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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); June7, 2018 {1}------------------------------------------------ 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 http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm. 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/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). 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 (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely. # Mary S. Runner -S forTina Kiang, Ph.D. Acting Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control, and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ### Indications for Use 510(k) Number (if known) K173573 Device Name Tetric® CAD Indications for Use (Describe) Tetric® CAD is intended for: - Veneers - Inalys - Onlays (e.g. occlusal veneers, partial crowns) - Crowns in the anterior and posterior region 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}------------------------------------------------ ### 510(K) SUMMARY Image /page/3/Picture/2 description: The image shows the logo for Ivoclar Vivadent, a dental company. The logo features the company name in a stylized font, with "Ivoclar" in green and "Vivadent" in blue. The tagline "passion vision innovation" is written in a smaller font below the company name. The logo also includes a series of green and blue dots and squares arranged in an arc above and to the right of the company name. | Contact: | Donna Hartnett, Director QA/Regulatory Ivoclar Vivadent, Inc. 175 Pineview Drive Amherst, New York 14228 716-691-2260 Donna.hartnett@ivoclarvivadent.com | |----------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Company: | Ivoclar Vivadent, AG Bendererstrasse 2, Schaan, FL-9494, Liechtenstein +423-235-3535 | | Date Prepared: | June 5, 2018 | | Proprietary Name: | Tetric® CAD | | Classification Name: | Material, Tooth Shade, Resin (872.3690) (Product Code: EBF) | | Predicate Device: | Cerasmart (K133824) by GC America, Inc. | Tetric® CAD is a composite block for the fabrication of esthetic Device Description: permanent inlays, onlays, veneers and crowns in the anterior and posterior region. Fabrication of the dental restoration is performed at the dentist's office in a compatible milling machine. The blocks are composed of cross-linked dimethacrylate and inorganic fillers. In the processing technique, the restoration is polished and seated after milling in the CAD/CAM system. The blocks are attached to a metal mandrel, the geometry of such is compatible with a milling machine, e.g. Cerec/InLab (Sirona), PlanMill (PlanMeca) or Programill One (Ivoclar Vivadent). Tetric® CAD composite blocks are available in the translucency levels MT (5 shades - A1, A2, A3, A3.5, BL) and HT (4 shades 0 A1, A2, A3, A3.5), and in the sizes I12 and C14. Indications for Use: Tetric® CAD is intended for: - Veneers " - -Inalys - -Onlays (e.g. occlusal veneers, partial crowns) - Crowns in the anterior and posterior region - {4}------------------------------------------------ K173573 Image /page/4/Picture/1 description: The image shows the logo for Ivoclar Vivadent. The logo is in blue and green, with the words "Ivoclar" and "Vivadent" stacked on top of each other. Above the words are a series of green dots and squares. The logo is simple and modern, and it is likely used to represent the company's brand. 510(K) SUMMARY Comparison to Predicate: The primary predicate devices to which Tetric® CAD has been compared is GC Americ a's Cerasmart (K133824). | Device | GC America: Cerasmart (K133824) | Ivoclar Vivadent: Tetric® CAD (K173573) | |----------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Indications for Use | The product is indicated for inlays, onlays, veneers and full crown restorations, including crowns on implants. | Tetric® CAD is intended for: - Veneers - Inlays - Onlays (e.g. occlusal veneers, partial crowns) - Crowns in the anterior and posterior region | | Precaution Measures/ Contraindications/ Processing restrictions/ Side effects | In rare cases this product may cause sensitivity in some people. If such reactions are experienced, discontinue the use of product and consult a physician. Personal protective equipment such as gloves, face masks and safety eyewear should always be worn. | Contraindications: - Bridge constructions - Conventional and self-adhesive cementation - Temporary cementation - Patients with severely reduced residual dentition - Any other use not listed in the indications Failure to observe the following restrictions may compromise the results achieved with Tetric® CAD: - Falling short of the required minimum layer thicknesses - Milling the blocks in a non-compatible CAD/CAM system - Deviations from the recommended luting protocol If a patient is known to be allergic to any of the ingredients of Tetric® CAD, the material should not be used. Do not inhale the composite resin dust during finishing. Use suction equipment and wear a dust mask | | Summary of Indications, Precaution Measures/ Contraindications/ Processing restrictions/ Side effects | The precautions, processing restrictions and contraindications are described in more detail for Tetric® CAD, but in total the indications and contraindications are substantially equivalent. | | | Technology | Cerasmart is a pre-cured composite block for milling CAD/CAM indirect restorations. The milled device is used for the restorations of both anterior and posterior teeth. | Tetric® CAD is a composite block for the fabrication of permanent inlays, onlays, veneers and crowns in the anterior and posterior region. In this processing technique, the restoration is polished and incorporated immediately after milling in the CAD/CAM system. | | Summary of Technology Delivery forms/dosage | The devices are similar, there is a minor difference in the wording. The blocks are available in 3 sizes (12, 14, 14L) in 33 shades (Translucency HT, LT and one Bleach shade). | The blocks are available in the translucency levels MT and HT, in 5 and 4 shades respectively, and in the sizes I12 and C14. | | Summary of Delivery forms/dosage | The predicate device is available in 3 sizes, one more than Tetric® CAD (14L is not available for Tetric® CAD). Additionally the predicate device offers 33 shades (Translucency HT, LT and a Bleach shade), Tetric® CAD offers 5 shades for MT and 4 shades for HT. Even though less shades are available the dentist can still meet the aesthetic demands of the patient. | | | Storage Conditions | Storage at room temperature (4 - 25 $^{\circ}$ C/39.2 - 77.0 $^{\circ}$ F), away from direct sunlight and high humidity; Shelf life: 5 years from date of manufacture | Storage conditions: 2 - 28 $^{\circ}$ C/36 - 82 $^{\circ}$ F, avoid sunlight Shelf life: 36 months | | Summary of Storage Conditions | The recommended shelf life is shorter for the new product, as less data is currently available. | | | Principles of Operation | Step by Step: -Preparation Design, shade selection -Scanning and Milling -Finishing and polishing -Characterization -Pre-Treatment -Cementation -Maintenance and repair | Step by Step: - Preparation, shade determination - Intraoral imaging, CAD/CAM process - Polishing - Characterization - Preparing for cementation - Cementation - Checking the articulation/occlusion, polishing - Aftercare | | Summary Principles of operation | There are minor differences in the wording between the predicate and the new product Tetric® CAD, but these are not significant and the principle of the operation is substantially equivalent. | | | Summary Chemical Composition | Both products are pre-cured composite blocks with differences in composition. Tetric® CAD has evaluated biocompatibility according to ISO 10993- 1:2009. | | | Finished Device Specification | Applicable standard: No information Applicable FDA Guidance: No information | EN 1641:2009 – Dentistry - Medical devices for dentistry - Materials Dental Composite Resin Devices – Premarket Notification [510(k)] Submission | | Sensitivity to light | Not relevant - industrially cured | Not relevant - industrially cured | | Color stability | Not relevant - industrially cured | Not relevant - industrially cured | | Flexural Strength | Brochure: 238 MPa | Typical mean value (IFU): 272 MPa | | Sterilization | Not applicable. No sterilization recommendation. | Not applicable. No sterilization recommendation. | | Single use | Consumable material | Consumable material | | Summary of Finished Device Specification | Tetric® CAD fulfils the relevant standard and follows the relevant Guidance. | | | Summary of Performance Specification | The value for flexural strength of Cerasmart (GC`s brochure) correlates with Ivoclar Vivadent's Tetric® CAD. | | {5}------------------------------------------------ ## 510(K) SUMMARY Image /page/5/Picture/2 description: The image shows the logo for Ivoclar Vivadent. The logo is in two lines, with "ivoclar" on the first line and "vivadent" on the second line. The word "ivoclar" is in green, and the word "vivadent" is in blue. There is a series of green and blue dots above the word "ivoclar". 3 #### Substantial equivalence to the predicate: The subject and the predicate device are pre-cured composite blocks for milling CAD/CAM restorations. Thus, the devices have the same function, have similar principles of operation and a similar chemical composition. The forgoing comparison supports that the subject device is substantially equivalent to the predicate device. #### Differences : The recommended storage temperature is marginally different (2-28 °C) compared to 4-25 °C for the predicate device. This is not substantial and is due to company policy. The shelf life is shorter (36 months) compared to 5 years for the predicate device. This is not substantial and is due to ongoing real-time testing. {6}------------------------------------------------ ### 510(K) SUMMARY Image /page/6/Picture/2 description: The image shows the logo for Ivoclar Vivadent, a dental company. The logo features the company name in a stylized font, with "Ivoclar" in a darker blue and "Vivadent" in a lighter blue. Above the company name is a series of green and blue dots arranged in an arc. Below the company name is the slogan "passion vision innovation" in a smaller font. The chemical composition is not fully published for the predicate device and therefore it is assumed there is some difference in ingredients, although the published data shows both products to be substantially equivalent. #### Non-clinical performance testing: Bench testing was performed to test the physical properties included in the Finished Device Specification for the subject device including: water solubility according to ISO 10477:2004 and flexural strength according to ISO 6872:2015. The subject device was tested in direct comparison to the predicate device and the results of the bench testing show the products to be substantially equivalent. #### Biocompatibility: The subject device was also evaluated for Biocompatibility according to ISO 10993-1:2009 +AC:2010. The following testing was conducted on the subject device: Cytotoxicity according to EN ISO 7405:2008 + A1:2013; ISO 10993-5:2009 and Genotoxicity according to 10993-3:2014 and the device was found to be non-cytotoxic and non-genotoxic. Conclusion: The data show that Tetric® CAD is substantially equivalent to the predicate device.