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FDA 510(k)

IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM

K-Number: K922779 · 1993-01-28

ApplicantAdvanced Implant Technologies, Inc.
Decision Date1993-01-28
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Implant Technologies, Inc.. It received FDA 510(k) clearance on 1993-01-28 under 510(k) number K922779. 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 IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM?

IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1993-01-28. The listed applicant is Advanced Implant Technologies, Inc.. The 510(k) number is K922779.

When did IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM receive FDA 510(k) clearance?

IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM received FDA 510(k) clearance on 1993-01-28, under 510(k) number K922779.

Who is the listed applicant for IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM?

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

What is the FDA product code for IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM?

The FDA product code for IMPLANT-PROPHY & PLASTIC DENTAL INSTRUMENT SYSTEM 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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