← Product Code [EIH](/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH) · K043462 # CZR PRESS LF (K043462) _Noritake Co., Inc. · EIH · Jan 11, 2005 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH/K043462 ## Device Facts - **Applicant:** Noritake Co., Inc. - **Product Code:** [EIH](/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH.md) - **Decision Date:** Jan 11, 2005 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.6660 - **Device Class:** Class 2 - **Review Panel:** Dental - **Attributes:** Therapeutic ## Indications for Use For use in prosthetic dentistry to create an all-ceramic prosthesis ## Device Story CZR Press LF is a dental porcelain powder used in prosthetic dentistry to create all-ceramic prostheses. The device is intended for professional use by dental technicians or dentists in a laboratory or clinical setting. It functions as a restorative material to replace missing tooth structure or restore dental aesthetics and function. The material is processed by the clinician to form the final prosthetic device. It benefits patients by providing a durable, aesthetic, and biocompatible solution for dental restoration. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Porcelain powder for clinical use; classified under 21 CFR 872.6660; Product Code EIH. ## 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. ## 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}------------------------------------------------ Image /page/0/Picture/2 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a stylized eagle or bird-like figure with three curved lines representing its wings or feathers. The bird is positioned to the right of the text, which is arranged in a circular pattern around the left side of the logo. The text reads "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA". JAN 1 1 2005 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Noritake Company, Incorporated C/O Mr. Ivan J. Wasserman, Counsel Collier Shannon Scott, PLLC Washington Harbour, Suite 400 3050 K Street NW Washington, District of Columbia 20007 Re: K043462 Trade/Device Name: CZR Press LF Regulation Number: 21 CFR 872.6660 Regulation Name: Porcelain Powder for Clinical Use Regulatory Class: II Product Code: EIH Dated: December 14, 2004 Received: December 15, 2004 Dear Mr Wasserman: We have reviewed your Section 510(k) premarket notification of intent to market the device We have reviewed your Section 510(x) pic.harter is substantially equivalent (for the indications for referenced above and have delemined the ace rices marketed in interstate commerce use stated in the enclosure) to legally market devices marketed in interstate use stated in the enclosure) to legally filanced produce Amendments, or to devices that prior to May 28, 1976, the enacthen with the provisions of the Federal Frod, Drug, and Cosmetic have been reclassified in accordance with the provisions of the Federal From W have been reclassified in accordance with the provisions of the Act. The mays. Act (Act) that do not require approval of a premarket approval applications of the general Act (Act) that do not require apploval of a prematice applo realizions of the Act. The general therefore, market the device, subject to the general controls provisions of de therefore, market the device, subject to the senents for annon registration, listing of devices, good controls provisions of the Act include requirements for annial registeri controls provisions of the Act mender requirements are at adulteration. 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 If your device is classified (see above) into Club Class in (erest ons affecting your device can be may be subject to such additional controls. Existing major regulations F may be subject to such additions, Title 21, Parts 800 to 89%. In addition, FDA may publish found in the Code of Federal Regulations, Title 21, Parts 800 to 89%. In additio found in the Code of Federal reegalament, your device in the Federal Register. {1}------------------------------------------------ ## Page 2 - Mr. Ivan J. Wasserman, Esq. Please be advised that FDA's issuance of a substantial equivalence determination does not mean Please be advised that I DA s issualled of a solenice complies with other requirements of the Act or that FDA made a decemination max your ced by other Federal agencies. You must comply with ally rederal statutes and regulations abut not limited to: registration and listing (21 CFR Part 807); all the Act s requirements, monacturing practice requirements as set forth in the quality labeling (21 CFR Part 001), good management of any from 11 case on one product radiation systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product Systems (QD) 105-105-131-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 510(k) I his letter will anow you to ocgin maneting your antial equivalence of your device to a legally premarket nothleation: "The FDA midning of backanse of 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 If you desire specific advice ion your ac now to 2011-01-11 5. Also, please note the regulation entitled, comact the Office of Comphance at (210) 27 of CFR Part 807.97). You may obtain other Misoraliums of reference to promaibilities under the Act from the Division of Small general intornation on your responsionnes 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, Carl S. Luip, Ph.D. Chiu S. Lin, PhD Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## Indications for Use 1043462 510(k) Number (if known): Device Name: CZR Press LF Indications For Use: For use in prosthetic dentistry to create an all-ceramic prosthesis Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Syoom Russe (Division Sign-Off) Division of Anesthesiology, General Hospital, Infection Control, Dental Devices Page 1 of _ | Kouzyler 510(k) Number:_ 7 --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH/K043462](https://fda.innolitics.com/submissions/DE/subpart-g%E2%80%94miscellaneous-devices/EIH/K043462) **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