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FDA 510(k)

ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING

K-Number: K992334 · 1999-10-08

Decision Date1999-10-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING is the device name listed in this FDA 510(k) record. The listed applicant is Implant Innovations, Inc.. It received FDA 510(k) clearance on 1999-10-08 under 510(k) number K992334. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING?

ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING is a medical device that received FDA 510(k) clearance on 1999-10-08. The listed applicant is Implant Innovations, Inc.. The 510(k) number is K992334.

When did ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING receive FDA 510(k) clearance?

ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING received FDA 510(k) clearance on 1999-10-08, under 510(k) number K992334.

Who is the listed applicant for ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING?

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

What is the FDA product code for ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING?

The FDA product code for ENDOSSEOUS IMPLANTS AND ABUTMENTS- TIN COATING is DZE.

Related Clinical Trials

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.

Other records listing Implant Innovations, 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.

View all 51 devices →

Related Devices (Code: DZE)

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.

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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