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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
What Zest Anchors, LLC makes
Zest Anchors, LLC manufactures dental implant suprastructures, fluted surgical drill bits, screw endosteal dental implants, surgical screwdrivers, dental soft-tissue coring punches, carbide dental burs, dental implant analogs, and dental surgical probes, all of which are reusable or preformed devices used in dental implant procedures.
These devices are classified as Class I and Class II medical devices and are listed in the FDA UDI registry; the company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of devices does Zest Anchors, LLC manufacture?
Zest Anchors, LLC manufactures dental implant suprastructures, fluted surgical drill bits, screw endosteal dental implants, surgical screwdrivers, dental soft-tissue coring punches, carbide dental burs, dental implant analogs, and dental surgical probes. These devices are used in dental implant procedures and are either preformed or reusable, as specified in the device data.
Where is Zest Anchors, LLC based?
Zest Anchors, LLC is based in the United States, as indicated by the COUNTRY field in the device data, which specifies US.
In which regulatory registry are Zest Anchors, LLC's devices listed?
Zest Anchors, LLC's devices are listed in the FDA UDI registry, as stated in the LISTED IN field of the device data, which identifies fda_udi as the registry.
How are Zest Anchors, LLC's devices classified under regulatory frameworks?
Zest Anchors, LLC's devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the device data, which lists both Class I and Class II as the applicable classifications.
AI-generated from registry data and not verified by a human reviewer.
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 9 of 70| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LOCATOR R-Tx | 31302-02 | FDA UDI | Class II | Active |
| Locator | 02969 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30502-03-AO | FDA UDI | Class II | Active |
| Locator | 08611 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 31600-04 | FDA UDI | Class II | Active |
| Locator | 01961 | FDA UDI | Class II | Active |
| SATURNO Narrow Diameter Implant System | 07715 | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 11302-05 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30510-03 | FDA UDI | Class II | Active |
| Locator | 07534 | FDA UDI | Class I | Active |
| Locator | 02362 | FDA UDI | Class II | Active |
| Chairside | 09580 | FDA UDI | Class I | Active |
| Locator | 01844 | FDA UDI | Class II | Active |
| Locator | 01285 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30301-04 | FDA UDI | Class II | Active |
| Locator | 01109 | FDA UDI | Class II | Active |
| LOCATOR, compatible with Anthogyr System | 08547 | FDA UDI | Class I | Active |
| Locator | 02241 | FDA UDI | Class II | Active |
| Locator | 01561 | FDA UDI | Class II | Active |
| LOCATOR, compatible with Implant Direct | 02078 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30201-00-AO | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30402-05 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 31500-01 | FDA UDI | Class II | Active |
| Locator | 08344 | FDA UDI | Class II | Active |
| Locator | 01283 | FDA UDI | Class II | Active |
| LOCATOR Overdenture Implant System | 07460 | FDA UDI | Class II | Active |
| LOCATOR Overdenture Implant System | 07450 | FDA UDI | Class II | Active |
| Locator | 02718 | FDA UDI | Class II | Active |
| Locator | 07533 | FDA UDI | Class I | Active |
| Locator | 01853 | FDA UDI | Class II | Active |
| Locator | 08992 | FDA UDI | Class II | Active |
| Locator | 08191 | FDA UDI | Class II | Active |
| Locator | 01224 | FDA UDI | Class II | Active |
| LOCATOR Overdenture Implant System | 07504 | FDA UDI | Class II | Active |
| Locator | 08233 | FDA UDI | Class II | Active |
| Locator | 01756 | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 10901-01 | FDA UDI | Class II | Active |
| LOCATOR F-Tx | 11713-03 | FDA UDI | Class II | Active |
| Locator | 01656 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30306-01 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30700-01 | FDA UDI | Class II | Active |
| LOCATOR, compatible with Ankylos System | 01729 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 32401-06 | FDA UDI | Class II | Active |
| LOCATOR R-Tx | 30706-06-AO | FDA UDI | Class II | Active |
| LOCATOR, Dentsply Sirona System | 30030-01 | FDA UDI | Class I | Active |
| Locator | 02980 | FDA UDI | Class II | Active |
| LOCATOR, compatible with Implant Direct | 08517 | FDA UDI | Class I | Active |
| LOCATOR F-Tx | 10502-01 | FDA UDI | Class II | Active |
| Locator | 07951 | FDA UDI | Class I | Active |
| LOCATOR F-Tx | 10701-02 | 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.
Zest Anchors, LLC has three recall records, with the earliest initiated on April 9, 2008, and the most recent on November 22, 2019. The statuses of these recalls are recorded as open, classified, and terminated. The reasons given for the recalls include a fit issue with Locator Abutments for 5.7 Screw-vent & Compatibles in certain Zimmer Dental implants, a labeling discrepancy regarding the recommended torque of 30 N-cm for LOCATOR Implant Attachment Systems, and the potential for abutments to be out of specification, which could result in a small gap between the implant and abutment during assembly.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| 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 |