← Product Code [EIH](/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH) · K041707 # CERCON CERAM EXPRESS CERAMIC SYSTEM (K041707) _Dentsply Intl. · EIH · Jul 30, 2004 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH/K041707 ## Device Facts - **Applicant:** Dentsply Intl. - **Product Code:** [EIH](/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH.md) - **Decision Date:** Jul 30, 2004 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 872.6660 - **Device Class:** Class 2 - **Review Panel:** Dental ## Indications for Use Designed for use on zirconia (zirconium oxide) in single tooth or bridge type restorations. Applications include tooth anterior and posterior locations. ## Device Story Dental ceramic veneering material; used for veneering zirconium oxide substructures for fixed prosthodontics (anterior/posterior crowns and bridges). Material: glass/glass-ceramic mixture; translucent and opaque components. Processing: medium-pressure, lost-wax injection molding (pressing) process. Used by dental professionals in clinical/laboratory settings to create aesthetic restorations. Output: finished ceramic veneer on zirconia substrate. Benefit: provides aesthetic and functional restoration for dental patients. ## Technological Characteristics Glass/glass-ceramic veneering material for zirconia substrates. Processing: medium-pressure, lost-wax injection molding (pressing). Modification of existing porcelain powder technology (21 CFR 872.6660). ## Regulatory Identification Porcelain powder for clinical use is a device consisting of a mixture of kaolin, felspar, quartz, or other substances intended for use in the production of artificial teeth in fixed or removable dentures, of jacket crowns, facings, and veneers. The device is used in prosthetic dentistry by heating the powder mixture to a high temperature in an oven to produce a hard prosthesis with a glass-like finish. ## Predicate Devices - Cercon® Ceram S Porcelains ([K022796](/device/K022796.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}------------------------------------------------ # 510(k) SUMMARY JUL 3 0 2004 #### NAME & ADDRESS: K041707 DENTSPLY International Susquehanna Commerce Center 221 West Philadelphia Street York, PA 17405-0872 Telefax (717) 849-4343 CONTACT: P. Jeffery Lehn DATE PREPARED: June 18, 2004 TRADE OR PROPRIETARY NAME: CERCON® CERAM EXPRESS Ceramic System CLASSIFICATION NAME: Porcelain powder for clinical use (872.6660) Cercon® Ceram S Porcelains (K022796) PREDICATE DEVICE: DEVICE DESCRIPTION: The CERCON® CERAM EXPRESS Ceramic System consists of a dental ceramic veneering material developed for veneering zirconium oxide substructures for fixed prosthodontics devices that include both anterior and posterior crowns and bridges. The modified device is a glass/glass-ceramic mixture used to veneer zirconia substrates in a medium-pressure. lost-wax injection molding (pressing) process. The modified device consists of a translucent material and an opaque material. INTENDED USE: Designed for use on zirconia (zirconium oxide) in single tooth or bridge type restorations. Applications include tooth anterior and posterior locations. TECHNOLOGICAL CHARACTERISTICS: CERCON® CERAM EXPRESS Ceramic System represents a modification to Cercon® Ceram S Porcelains (K022796). Changes have been made to the device's formulation, material form, and processing technique. All of the components found in CERCON® CERAM EXPRESS Ceramic System have been used in legally marketed devices. We believe that the prior use of the components of CERCON® CERAM EXPRESS Ceramic System in legally marketed devices, the similarity in the formulations between the modified and the marketed device, and the data provided regarding the modifications to the marketed device support the safety and effectiveness of CERCON® CERAM EXPRESS Ceramic System for the intended use. {1}------------------------------------------------ Image /page/1/Picture/1 description: The image is a seal with the words "DEPARTMENT OF HEALTH & HUMAN JUSTICE - USA" arranged in a circle around a stylized image of an eagle. The eagle is facing right and has three curved lines representing its wings and body. The seal is black and white. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 ## JUL 3 0 2004 Mr. P. Jeffery Lehn Director, Corporate Compliance and Regulatory Affairs DENTSPLY, International Susquehanna Commerce Center 221 West Philadelphia Street, Suite 60 York, Pennsylvania 17404 Re: K041707 Trade/Device Name: CERCON® CERAM EXPRESS Ceramic System Regulation Number: 21 CFR 872.6660 Regulation Name: Porcelain Powder for Clinical Use Regulatory Class: II Product Code: EIH Dated: June 18, 2004 Received: June 23, 2004 Dear Mr. Lehn: 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 vour 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. {2}------------------------------------------------ Page 2 - Mr. Lehn 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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic 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 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 regulation (21 CFR Part 801), please contact the Office of Compliance at (301) 594-4613. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act 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 yours. Chi-Lin, Ph.D. Chiu Lin, Ph.D. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ #### INDICATIONS FOR USE STATEMENT (As Required by 21 CFR 807.87(e) Ko41707 510(K) Number (if known): ### Device Name: CERCON® CERAM EXPRESS Ceramic System Indications for Use: Designed for use on zirconia (zirconium oxide) in single tooth or bridge type restorations. Applications include tooth anterior and posterior locations. Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) #### (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Ken Morley (Divisio Divisio of Anesthesony Genera, nospital, Infection Control Dental Devices 510(k) Nuribe K041707 ー --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH/K041707](https://fda.innolitics.com/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH/K041707) **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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