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FDA 510(k)

ZEST ANCHOR ADVANCED GENERATION

K-Number: K925700 · 1994-04-07

ApplicantZest Anchors, Inc.
Decision Date1994-04-07
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZEST ANCHOR ADVANCED GENERATION is the device name listed in this FDA 510(k) record. The listed applicant is Zest Anchors, Inc.. It received FDA 510(k) clearance on 1994-04-07 under 510(k) number K925700. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEST ANCHOR ADVANCED GENERATION?

ZEST ANCHOR ADVANCED GENERATION is a medical device that received FDA 510(k) clearance on 1994-04-07. The listed applicant is Zest Anchors, Inc.. The 510(k) number is K925700.

When did ZEST ANCHOR ADVANCED GENERATION receive FDA 510(k) clearance?

ZEST ANCHOR ADVANCED GENERATION received FDA 510(k) clearance on 1994-04-07, under 510(k) number K925700.

Who is the listed applicant for ZEST ANCHOR ADVANCED GENERATION?

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

What is the FDA product code for ZEST ANCHOR ADVANCED GENERATION?

The FDA product code for ZEST ANCHOR ADVANCED GENERATION is EGG.

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Other records listing Zest Anchors, 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.

K083324LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEMK072878MODIFICATION TO: LOCATOR IMPLANT ANCHORK042466X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALEK033699LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586K994257LOCATOR IMPLANT ANCHORK925849ZEST IMPLANT ANCHOR

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Related Devices (Code: EGG)

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.

K990979STECO-TITANMAGNETICSSteco-System-Technik GmbH & CokgK950259COUPLING DEVICE FOR DENTAL PROSTHESISDr. Joseph E. Grasso, D.D.S.K915299COGAN CORP KITS OF DENTAL HAND INSTRUMENTSCogan Corp.K912435DENTAL CONNECTOR PRECISION ATTACHMENTMetalor Dental USA Corp.K912567CONICAST, INTRACAST, OMECASTMetalor Dental USA Corp.K901928INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACHInterpore Intl.

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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