K250721
- 510(k) number
- K250721
- Device name
- LOCATOR® Angled Abutment
- Applicant
- Zest Anchors, LLC CA · US
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-08-20
- Date received
- 2025-03-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K250721.pdf
Official FDA record: K250721
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.