LOCATOR® Angled Abutment
K-Number: K260555 · 2026-04-09
ApplicantZest Anchors, LLC
Decision Date2026-04-09
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 2026-04-09 under approval number K260555. 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 2026-04-09. It is manufactured by Zest Anchors, LLC. The 510(k) number is K260555.
When was LOCATOR® Angled Abutment approved by the FDA?
LOCATOR® Angled Abutment received FDA 510(k) clearance on 2026-04-09, under approval number K260555.
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.
Other Devices by Zest Anchors, LLC
Related Devices (Code: NHA)
K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd.
K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG
K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A.
K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd.
K161435Temporary Snap AbutmentNobel Biocare AB
K160786RODO Abutment SystemRodo Medical, 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.