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FDA 510(k)

VERABOND III

K-Number: K945714 · 1994-12-29

ApplicantAalba Dent, Inc.
Decision Date1994-12-29
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERABOND III is the device name listed in this FDA 510(k) record. The listed applicant is Aalba Dent, Inc.. It received FDA 510(k) clearance on 1994-12-29 under 510(k) number K945714. 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 VERABOND III?

VERABOND III is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K945714.

When did VERABOND III receive FDA 510(k) clearance?

VERABOND III received FDA 510(k) clearance on 1994-12-29, under 510(k) number K945714.

Who is the listed applicant for VERABOND III?

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

What is the FDA product code for VERABOND III?

The FDA product code for VERABOND III is EJH.

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Other records listing Aalba Dent, 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.

K040180CONTINUM VK040179CONTINUMK033356VERASOFT ESK982094VERABOND 2K972971NPG + 2K973265VERABOND 2V

View all 27 devices →

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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