FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LOCATOR® Angled Abutment

K Number: K250721 · Decision Aug 20, 2025
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
12
Review Days
163

Basic Information

Device Name
LOCATOR® Angled Abutment
K Number
K250721
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zest Anchors, LLC
Date Received
March 10, 2025
Decision Date
August 20, 2025
Product Code
NHA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NHA Abutment, Implant, Dental, Endosseous

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Other Clearances by Zest Anchors, LLC

K Number Device Name
K260555 LOCATOR® Angled Abutment
K252944 LOCATOR® Angled Abutment
K243272 LOCATOR Angled Abutment
K233587 LOCATOR Angled Abutment (Various)
K220252 High Retention Attachment System
K213391 High Retention Attachment System
K191619 TurboTemp EZ
K151789 LOCATOR F-Tx Attachment System
K133327 SATURNO(TM) OVERDENTURE IMPLANT SYSTEM
K140570 CHAIRSIDE ATTACHMENT PROCESSING MATERIAL
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