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Sign in to claim this brandZest Anchors, LLC
United States·US-MF-000009815
Last updated September 17, 2026
About
ZEST Dental Solutions has been manufacturing overdenture implant attachment systems as a global leader and being one of the top dental implant manufacturers for over forty years.
From the manufacturer's own website. Source
Information
- Country
- United States
- Address
- 2875, Loker Avenue East, Carlsbad, United States
- Website
- www.zestdent.com/
- linkedin.com/company/zest-anchors
- facebook.com/ZestDentalSolutions
- [email protected]
- Phone
- +1 760 743 7744
- PRRC Contact
- Maleata Hall
- EUDAMED SRN
- US-MF-000009815
- FDA FEI Number
- 2023950
- DUNS Number
- —
Catalogue (3457)
Page 4 of 70| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LOCATOR Fixed, compatible with Implant Direct | 10159-01 | FDA UDI | Class I | Active |
| LOCATOR F-Tx | 10810-03 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30900-06 | FDA UDI | Class II | Active |
| Locator | 08721 | FDA UDI | Class II | Active |
| Locator | 08021 | FDA UDI | Class II | Active |
| Locator | 02406 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 31111-03 | FDA UDI | Class II | Active |
| LOCATOR Overdenture Implant System | 07513-05 | FDA UDI | Class II | Active |
| Locator | 08461 | FDA UDI | Class II | Active |
| LOCATOR Overdenture Implant System | 07475 | FDA UDI | Class II | Active |
| Locator | 08321 | FDA UDI | Class II | Active |
| Locator | 08822 | FDA UDI | Class II | Active |
| Locator | 01352 | FDA UDI | Class II | Active |
| Locator | 02226 | FDA UDI | Class II | Active |
| Locator | 01770 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30416-04 | FDA UDI | Class II | Active |
| Locator | 07546 | FDA UDI | Class I | Active |
| Locator | 01192 | FDA UDI | Class II | Active |
| Locator | 01063 | FDA UDI | Class II | Active |
| Locator | 07982 | FDA UDI | Class I | Active |
| Locator | 01235 | FDA UDI | Class II | Active |
| Locator | 08100 | FDA UDI | Class II | Active |
| Locator | 02004 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30502-01 | FDA UDI | Class II | Active |
| Locator | 01995 | FDA UDI | Class II | Active |
| Locator | 01212 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30206-06 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 31112-04 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30202-01-AO | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 11801-06 | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 10036-01 | FDA UDI | Class I | Active |
| Locator | 08693 | FDA UDI | Class II | Active |
| Locator | 07368 | FDA UDI | Class I | Active |
| LOCATOR R-Tx | 30301-02-AO | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 10600-02 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30600-04-AO | FDA UDI | Class II | Active |
| Locator | 08020 | FDA UDI | Class II | Active |
| Locator | 01215 | FDA UDI | Class II | Active |
| LOCATOR Overdenture Implant System | 07452 | FDA UDI | Class II | Active |
| Locator | 01624 | FDA UDI | Class II | Active |
| LOCATOR, compatible with Implant Direct | 08529 | FDA UDI | Class I | Active |
| LOCATOR R-Tx | 32100-01 | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 10801-02 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 31801-04 | FDA UDI | Class II | Active |
| Locator | 02240 | FDA UDI | Class II | Active |
| Locator | 02985 | FDA UDI | Class II | Active |
| Locator | 08696 | FDA UDI | Class II | Active |
| Locator | 01660 | FDA UDI | Class II | Active |
| Locator | 01428 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30306-05 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
- MDSS GmbH DE
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 22, 2019 | Z-2425-2020 | — | open, classified | The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient. |
| Jan 16, 2014 | Z-0935-2014 | — | terminated | Zest Anchors, LLC is voluntarily recalling specific lots of LOCATOR Implant Attachment Systems because it is currently provided with a label that indicates that the final torque applied to the abutment should be 30 N-cm. It was recently noted by Zest that in order to provide an optimal performance by increasing the factor of safety between the failure load of the abutment screw and the recommend |
| Apr 9, 2008 | Z-0298-2009 | — | terminated | The recall was initiated after the firm discovered through a customer complaint that the Locator Abutments for 5.7 Screw-vent & Compatibles do not fit properly in all sizes of the Zimmer Dental 5.7mm diameter Tapered Screw-Vent Implants (TSV6B8, TSV6B10, TSV6B11, TSV6B13, TSV6B16, TSV6H8, TSV6H10, TSV6H11, TSV6H13 and TSV6H16). The Locator Abutment bottoms out in the pilot hole of these implants c |