← Product Code [KLE](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE) · K020514 # PULPDENT GLAZE II (K020514) _Pulpdent Corporation · KLE · May 16, 2002 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE/K020514 ## Device Facts - **Applicant:** Pulpdent Corporation - **Product Code:** [KLE](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE.md) - **Decision Date:** May 16, 2002 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.3200 - **Device Class:** Class 2 - **Review Panel:** Dental ## Intended Use Pulpdent Glaze II is a light-cured, unfilled resin that contains no Bisphenol A and is used as a penetrating composite sealer and bonding agent. Pulpdent Glaze II bonds to composite and etched enamel, seals composite margins, penetrates and seals composite surface, reducing micro-leakage, wear and marginal breakdown. ## Device Story Pulpdent Glaze II is a light-cured, unfilled resin dental material. It functions as a penetrating sealer and bonding agent for composite restorations and etched enamel. Applied by dental professionals in a clinical setting, the material penetrates composite surfaces and seals margins to reduce micro-leakage, wear, and marginal breakdown. It is formulated without Bisphenol A. The device is used to improve the longevity and integrity of dental composite restorations. ## Clinical Evidence No clinical data. Substantial equivalence is supported by laboratory testing demonstrating physical and mechanical property equivalence to predicate devices and historical usage data for similar dental restorative materials. ## Technological Characteristics Light-cured, unfilled resin material. Formulated without Bisphenol A. Functions as a surface sealant and bonding agent. No specific ASTM/ISO standards cited. ## Regulatory Identification A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be painted on the interior of a prepared cavity of a tooth to improve retention of a restoration, such as a filling. ## Predicate Devices - Pulpdent Resin Bonding Agent - Bisco Fortify - UltraDent PermaSeal ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ PULPDENT CORPORATION ## MAY 1 6 2002 KO20514 #### EXHIBIT 2 #### SUMMARY OF SAFETY AND EFFECTIVENESS DATA Kenneth J. Berk 80 Oakland Street PO Box 780 Watertown, MA 02472 USA 617-926-6666 Telephone: Fax: 617-926-6262 ken@pulpdent.com DEVICE: Trade Name: PULPDENT GLAZE II Classification Name: Agent, Tooth Bonding, Resin FDA Product Code: 76 KLE, 21 CFR Part 872.3200 #### PREDICATE DEVICE: Pulpdent Resin Bonding Agent Bisco Fortify UltraDent PermaSeal #### DESCRIPTION AND INTENDED USE: Pulpdent Glaze II is a light-cured, unfilled resin that contains no Bisphenol A and is used as a penetrating composite sealer and bonding agent. Pulpdent Glaze II bonds to composite and etched enamel, seals composite margins, penetrates and seals composite surface, reducing micro-leakage, wear and marginal breakdown. #### COMPARISON WITH PREDICATE PRODUCTS: PULPDENT GLAZE II substantially equivalent in design, composition, performance, intended use, safety and effectiveness to the predicate products listed above. #### SAFETY AND EFFECTIVENESS: PULPDENT GLAZE II is substantially equivalent in design, composition, performance, intended use, safety and effectiveness to the predicate products listed above. The predicate products have been found substantially equivalent under the 510(k) premarket notification process as Class II Dental Devices under CFR 872.3200. Though there is no ISO or ANSI/ADA standard applicable to Pulpdent Glaze II, laboratory testing has shown that Pulpdent Glaze II is equivalent in physical and mechanical properties to the predicate products, According to the NH Technology Assessment Conference on Effects and Side-Effects of Dental Restorative Materials: "General usage of these materials over about 20 years indicates a high benefit-torisk ratio...both composites and glass ionomers are relatively trouble-free. There is no evidence of shortterm or long-term risk...There is no suspicion of any problems after virtually billions of procedures in the United States. 7 {1}------------------------------------------------ ## DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 # MAY 1 6 2002 Mr. Kenneth J. Berk Director Pulpdent Corporation 80 Oakland Street Watertown, Massachusetts 02472 Re: K020514 Trade/Device Name: Pulpdent Glaze II Regulation Number: 21 CFR 872.3200 Regulation Name: Agent, Tooth Bonding, Resin Regulatory Class: II Product Code: KLE Dated: February 12, 2002 Received: February 15, 2002 Dear Mr. Berk: 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. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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 {2}------------------------------------------------ Page 2 - Mr. Berk and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice alle libang (21 CFF an in the quality systems (QS) regulation (21 CFR Part 820); and if requirements as between a product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 110(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 n you debire ope 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html Sincerely, Patricia Curente /for Timothy A. Ulatowski Director Division of Dental, Infection Control and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ ## INDICATIONS FOR USE STATEMENT K020514 510 (k) Number (if known) PULPDENT GLAZE II Device Name Indications for Use: Pulpdent Glaze II is a light-cured, unfilled resin that contains no Bisphenol A and is r alpaon. One if to a light sealer and bonding agent. Pulpdent Glaze II bonds to composite and etched enamel, seals composite margins, penetrates and seals composite surface, reducing micro-leakage, wear and marginal breakdown. Please do not write below this line. Continue on another page if needed. Concurrence of CDRH, Office of Device Evaluation (ODE) Susan Runne Division Sign-Off fon of Dental, Infection Control, and General Hospital Devices 510(k) Number K020514 Prescription Use レ (Per 21 CFR 801.109) - or Over-The-Counter Use 5 --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE/K020514](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE/K020514) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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