Zest Anchors, LLC
Zest Anchors, LLC holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2026, with 2 FDA device recalls on record.
Top product codes for Zest Anchors, LLC
FDA recalls by Zest Anchors, LLC
- Z-2425-2020 — LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 .
- Z-0935-2014 — LOCATOR¿ Implant Attachment System. The LOCATOR¿ Implant Attachment System is a universal hinge, resilient attachment for endosseous implants. The LOCATOR¿ Implant Attachment System is designed for use with overdentures or partial dentures, retained in whole or in part, by endosseous implants in the mandible or maxilla. FDA 510(k): K994257, K072878
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Zest Anchors, LLC
- K260555 — LOCATOR® Angled Abutment
- K252944 — LOCATOR® Angled Abutment
- K250721 — 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
- K120198 — LOCATOR OVERDENTURE IMPLANT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.