Data / Medical devices / United States / Zest Anchors, LLC
Zest Anchors, LLC: FDA-registered device maker in Escondido, CA, United States, 19 510(k) clearances
Zest Anchors, LLC is registered with the FDA (registration 3006796211) in Escondido, CA, United States. It lists 5 device types. The FDA files 19 510(k) clearances under its listings, the newest dated April 9, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3006796211
- Address
- 2230 Enterprise Street, Escondido, CA, United States, 92029
- Owner or operator
- Zest Anchors, LLC (2023950)
- Roles
- Manufacturer
- First device listed
- December 2, 1992
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Attachment, Precision, All | EGG | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Post, Root Canal | ELR | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 9, 2026 | K260555 | LOCATOR® Angled Abutment | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| October 15, 2025 | K252944 | LOCATOR® Angled Abutment | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| August 20, 2025 | K250721 | LOCATOR® Angled Abutment | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| January 14, 2025 | K243272 | LOCATOR Angled Abutment | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| June 3, 2024 | K233587 | LOCATOR Angled Abutment (Various) | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| April 14, 2022 | K220252 | High Retention Attachment System | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| January 11, 2022 | K213391 | High Retention Attachment System | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| April 15, 2021 | K203701 | Locator Overdenture Implant System | DZE | Substantially Equivalent | Ivory Super Holdco Inc. / Zest Anchors, LLC | accessdata.fda.gov |
| March 4, 2016 | K151789 | LOCATOR F-Tx Attachment System | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| July 24, 2015 | K150295 | LOCATOR RTx | NHA | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| June 25, 2014 | K133327 | SATURNO(TM) OVERDENTURE IMPLANT SYSTEM | DZE | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| June 6, 2012 | K120198 | LOCATOR OVERDENTURE IMPLANT SYSTEM | DZE | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| February 25, 2009 | K083324 | LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM | NHA | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| December 3, 2007 | K072878 | MODIFICATION TO: LOCATOR IMPLANT ANCHOR | NHA | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| April 22, 2004 | K033699 | LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 | DZE | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| September 28, 2001 | K012911 | 3I LOCATER ABUTMENT SYSTEM | DZE | Substantially Equivalent | Implant Innovations, Inc. | accessdata.fda.gov |
| March 17, 2000 | K994257 | LOCATOR IMPLANT ANCHOR | DZE | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| June 22, 1994 | K934668 | ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL) | DZE | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| April 7, 1994 | K925700 | ZEST ANCHOR ADVANCED GENERATION | EGG | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Attachment, Precision, All
- All makers of Post, Root Canal
Updated April 9, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.