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FDA 510(k)

ZEST PLANT

K-Number: K801524 · 1980-07-21

ApplicantZest Anchors, Inc.
Decision Date1980-07-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZEST PLANT 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 1980-07-21 under 510(k) number K801524. 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 ZEST PLANT?

ZEST PLANT is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Zest Anchors, Inc.. The 510(k) number is K801524.

When did ZEST PLANT receive FDA 510(k) clearance?

ZEST PLANT received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801524.

Who is the listed applicant for ZEST PLANT?

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 PLANT?

The FDA product code for ZEST PLANT 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.

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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

View all 13 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.

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

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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