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FDA 510(k)

REMATITAN TITANIUM

K-Number: K952866 · 1995-07-27

ApplicantDentauraum, Inc.
Decision Date1995-07-27
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REMATITAN TITANIUM is the device name listed in this FDA 510(k) record. The listed applicant is Dentauraum, Inc.. It received FDA 510(k) clearance on 1995-07-27 under 510(k) number K952866. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMATITAN TITANIUM?

REMATITAN TITANIUM is a medical device that received FDA 510(k) clearance on 1995-07-27. The listed applicant is Dentauraum, Inc.. The 510(k) number is K952866.

When did REMATITAN TITANIUM receive FDA 510(k) clearance?

REMATITAN TITANIUM received FDA 510(k) clearance on 1995-07-27, under 510(k) number K952866.

Who is the listed applicant for REMATITAN TITANIUM?

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

What is the FDA product code for REMATITAN TITANIUM?

The FDA product code for REMATITAN TITANIUM is EJH.

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Other records listing Dentauraum, Inc. 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.

K952867REMANIUM:GM 700, GM 380, GM 800, GFHK952870REMANIUM: CS & G-SOFTK952865REMANIUM: 200,CS, 380, AND CDK952868DENTAURUM JACKET CROWN & ROOT POSTSK942667DENT-O-CRYL ORTHODONTIC ACRYLICK942666ORTHALGENAT IMPRESSION MATERIAL

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Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K032136WIROBOND CBego U.S.A.

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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