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FDA 510(k)

DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC

K-Number: K001269 · 2000-06-21

ApplicantDentalmatic Technologies, Inc.
Decision Date2000-06-21
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC is the device name listed in this FDA 510(k) record. The listed applicant is Dentalmatic Technologies, Inc.. It received FDA 510(k) clearance on 2000-06-21 under 510(k) number K001269. 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 DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC?

DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC is a medical device that received FDA 510(k) clearance on 2000-06-21. The listed applicant is Dentalmatic Technologies, Inc.. The 510(k) number is K001269.

When did DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC receive FDA 510(k) clearance?

DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC received FDA 510(k) clearance on 2000-06-21, under 510(k) number K001269.

Who is the listed applicant for DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC?

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

What is the FDA product code for DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC?

The FDA product code for DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC is EJH.

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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

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

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