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FDA 510(k)

HD-4 CROWN & BRIDGE ALLOY

K-Number: K905034 · 1991-09-05

ApplicantHo Dental Co., Inc.
Decision Date1991-09-05
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HD-4 CROWN & BRIDGE ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Ho Dental Co., Inc.. It received FDA 510(k) clearance on 1991-09-05 under 510(k) number K905034. 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 HD-4 CROWN & BRIDGE ALLOY?

HD-4 CROWN & BRIDGE ALLOY is a medical device that received FDA 510(k) clearance on 1991-09-05. The listed applicant is Ho Dental Co., Inc.. The 510(k) number is K905034.

When did HD-4 CROWN & BRIDGE ALLOY receive FDA 510(k) clearance?

HD-4 CROWN & BRIDGE ALLOY received FDA 510(k) clearance on 1991-09-05, under 510(k) number K905034.

Who is the listed applicant for HD-4 CROWN & BRIDGE ALLOY?

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

What is the FDA product code for HD-4 CROWN & BRIDGE ALLOY?

The FDA product code for HD-4 CROWN & BRIDGE ALLOY 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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