LOCATOR® Angled Abutment
K-Number: K252944 · 2025-10-15
ApplicantZest Anchors, LLC
Decision Date2025-10-15
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 2025-10-15 under approval number K252944. 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 2025-10-15. It is manufactured by Zest Anchors, LLC. The 510(k) number is K252944.
When was LOCATOR® Angled Abutment approved by the FDA?
LOCATOR® Angled Abutment received FDA 510(k) clearance on 2025-10-15, under approval number K252944.
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.