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FDA 510(k)

VITAPAN ACRYLIC DENTURE TEETH

K-Number: K914476 · 1992-03-02

ApplicantVident
Decision Date1992-03-02
Product CodeELM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VITAPAN ACRYLIC DENTURE TEETH is the device name listed in this FDA 510(k) record. The listed applicant is Vident. It received FDA 510(k) clearance on 1992-03-02 under 510(k) number K914476. The device is classified under product code ELM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAPAN ACRYLIC DENTURE TEETH?

VITAPAN ACRYLIC DENTURE TEETH is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Vident. The 510(k) number is K914476.

When did VITAPAN ACRYLIC DENTURE TEETH receive FDA 510(k) clearance?

VITAPAN ACRYLIC DENTURE TEETH received FDA 510(k) clearance on 1992-03-02, under 510(k) number K914476.

Who is the listed applicant for VITAPAN ACRYLIC DENTURE TEETH?

The FDA 510(k) record lists Vident as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAPAN ACRYLIC DENTURE TEETH?

The FDA product code for VITAPAN ACRYLIC DENTURE TEETH is ELM.

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Other records listing Vident as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K063768TITANIUM SCALLOPED ABUTMENTK060441VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98K052710VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,K052130VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40K050362VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)K022996VITA IN-CERAM YZ CUBES FOR CEREC

View all 36 devices →

Related Devices (Code: ELM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K122955DENTAVIT, MONARCH, ACROTONE, SENATOR, DENTORIUMWright Health Group , Ltd.K122925NEW STETIC ARTIFICIAL TEETHNew SteticK122852PHYSIOSTAR NFCCandulor USA, Inc.K121749VERACIAShofu Dental CorporationK120404MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETHMerz Dental GmbHK120736SR PHONARES IIIvoclar Vivadent, AG

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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