← Product Code [KLE](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE) · K982007 # TRUBYTE DENTURE BOND DENTURE BONDING AGENT (K982007) _Dentsply Intl. · KLE · Jul 22, 1998 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE/K982007 ## Device Facts - **Applicant:** Dentsply Intl. - **Product Code:** [KLE](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE.md) - **Decision Date:** Jul 22, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.3200 - **Device Class:** Class 2 - **Review Panel:** Dental ## Intended Use TRUBYTE® DENTURE BOND Denture Bonding Agent is used to bond plastic denture teeth and denture reline materials to acrylic denture bases. ## Device Story TRUBYTE® DENTURE BOND is a polymer/monomer liquid solution used in dental laboratories or clinics. It functions as a bonding agent to adhere plastic denture teeth and reline materials to acrylic denture bases. The device is applied by dental professionals during the denture fabrication or repair process. It ensures structural integrity between the denture components. The product is chemically compatible with both heat-cured and auto-polymerizable acrylic denture base resins. Its use does not alter the residual monomer content of the denture base, ensuring safety for the patient. ## Clinical Evidence Bench testing only. Gas chromatographic analysis was performed on denture samples to compare residual methyl methacrylate monomer content in dentures prepared with and without the bonding agent. Results showed no statistically significant difference in residual monomer levels, confirming the agent does not adversely affect the denture base material. ## Technological Characteristics Polymer/monomer liquid solution. Compatible with heat-cured and auto-polymerizable acrylic denture base resins. No specific ASTM standards or complex software/connectivity features described. ## 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 - Palabond® Adhesion Primer ([K924422](/device/K924422.md)) ## 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}------------------------------------------------ .111 22 1998 K982667 DENTSPLY ## 510(k) SUMMARY DENTSPLY International 570 West College Avenue P.O. Box 872 York, PA 17405-0872 717) 845-7511 NAME & ADDRESS: P. J. Lehn Telefax (717) 849-4343 P. Jeffery Lehn CONTACT: DATE PREPARED: June 4, 1998 TRADE OR PROPRIETARY NAME: TRUBYTE® DENTURE BOND Denture Bonding Agent 872.3200 CLASSIFICATION NAME: Resin tooth bonding agent K924422 Palabond® Adhesion Primer PREDICATE DEVICES: DEVICE DESCRIPTION: TRUBYTE® DENTURE BOND Denture Bonding Agent is a polymer/ monomer liquid solution. It is compatible with both heat-cured and auto-polymerizable acrylic denture base resins. INTENDED USE: TRUBYTE® DENTURE BOND Denture Bonding Agent is used to bond plastic denture teeth and denture reline materials to acrylic denture bases. TECHNOLOGICAL CHARACTERISTICS: All of the components found in TRUBYTE® DENTURE BOND Denture Bonding Agent have been used in legally marketed medical devices. Gas chromatographic analysis of the residual methyl methacrylate monomer in denture samples was conducted to determine the effect that TRUBYTE® DENTURE BOND Denture Bonding Agent use would have on the residual monomer content in a denture. There is not a statistically significant difference in residual monomer between samples that utilized TRUBYTE® DENTURE BOND Denture Bonding Agent vs. those prepared without bonding agent. This analysis confirms that TRUBYTE® DENTURE BOND Denture Bonding Agent use does not affect the amount of residual monomer present in the denture base. Accordingly, no additional patient risk is associated with the use of TRUBYTE® DENTURE BOND Denture Bonding Agent on dentures properly processed with Lucitone® 199 or Lucitone® FasPor+™ pourable denture base. We believe that the prior use of the components of TRUBYTE® DENTURE BOND Denture Bonding Agent in legally marketed predicate devices, and the performance and safety data provided, support the safety and effectiveness of TRUBYTE® DENTURE BOND Denture Bonding Agent for the indicated uses. 00013 {1}------------------------------------------------ Image /page/1/Picture/1 description: The image contains the text 'Public Health Service'. The text is in a simple, sans-serif font and is horizontally aligned. The words are stacked on a single line. Image /page/1/Picture/2 description: The image shows the seal of the Department of Health & Human Services (HHS) of the United States of America. The seal features a stylized eagle with three stripes representing the three branches of government. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" are arranged in a circular pattern around the eagle. JUL 22 1998 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. P. Jeffrey Lehn ·Associate Director Corporate Compliance DENTSPLY International 570 West College Avenue P.O. Box 872 York, Pennsylvania 17404 Re: K982007 TRUBYTE® DENTURE BOND Denture Bonding Agent Trade Name: Requlatory Class : II Product Code: EBI June 4, 1997 Dated: Received: June 8, 1997 Dear Mr. Lehn: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act 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 (Premarket Approval), 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 895. ਜ substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. {2}------------------------------------------------ Page 2 - Mr. Lehn This letter will allow you to begin marketing your device as described in your 510(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 requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. 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" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, S. Butman Jr 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}------------------------------------------------ ## PREMARKET NOTIFICATION ## INDICATIONS FOR USE STATEMENT (As Required by 21 CFR 801.109) 510(K) Number: K982007 Device Name: TRUBYTE® DENTURE BOND Denture Bonding Agent TRUBYTE® DENTURE BOND Denture Bonding Agent is used to bond plastic denture teeth and denture reline materials to acrylic denture bases. Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use OR Over-The-Counter Use _________________________________________________________________________________________________________________________________________________________ Susan Russo (Division Sign-Off) Division of Dental, Infection Control, and General Hospital Pevice 510(k) Number_ 000007 --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE/K982007](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/KLE/K982007) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com