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FDA 510(k)

VARIOUS DENTAL IMPLANTS WITH COVER SCREWS

K-Number: K961861 · 1996-08-22

ApplicantImplant Management of America
Decision Date1996-08-22
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VARIOUS DENTAL IMPLANTS WITH COVER SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Implant Management of America. It received FDA 510(k) clearance on 1996-08-22 under 510(k) number K961861. 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 VARIOUS DENTAL IMPLANTS WITH COVER SCREWS?

VARIOUS DENTAL IMPLANTS WITH COVER SCREWS is a medical device that received FDA 510(k) clearance on 1996-08-22. The listed applicant is Implant Management of America. The 510(k) number is K961861.

When did VARIOUS DENTAL IMPLANTS WITH COVER SCREWS receive FDA 510(k) clearance?

VARIOUS DENTAL IMPLANTS WITH COVER SCREWS received FDA 510(k) clearance on 1996-08-22, under 510(k) number K961861.

Who is the listed applicant for VARIOUS DENTAL IMPLANTS WITH COVER SCREWS?

The FDA 510(k) record lists Implant Management of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIOUS DENTAL IMPLANTS WITH COVER SCREWS?

The FDA product code for VARIOUS DENTAL IMPLANTS WITH COVER SCREWS is DZE.

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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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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