LOCATOR® Angled Abutment
K-Number: K250721 · 2025-08-20
ApplicantZest Anchors, LLC
Decision Date2025-08-20
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
LOCATOR® Angled Abutment is a medical device manufactured by Zest Anchors, LLC. It received FDA 510(k) clearance on 2025-08-20 under approval number K250721. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LOCATOR® Angled Abutment?
LOCATOR® Angled Abutment is a medical device that received FDA 510(k) clearance on 2025-08-20. It is manufactured by Zest Anchors, LLC. The 510(k) number is K250721.
When was LOCATOR® Angled Abutment approved by the FDA?
LOCATOR® Angled Abutment received FDA 510(k) clearance on 2025-08-20, under approval number K250721.
What company makes LOCATOR® Angled Abutment?
LOCATOR® Angled Abutment is manufactured by Zest Anchors, LLC.
What is the FDA product code for LOCATOR® Angled Abutment?
The FDA product code for LOCATOR® Angled Abutment is NHA.
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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.