Data / Medical devices / United States / Zest Anchors, LLC
Zest Anchors, LLC: FDA-registered device maker in Carlsbad, CA, United States, 51 510(k) clearances
Zest Anchors, LLC is registered with the FDA (registration 2023950) in Carlsbad, CA, United States. It lists 29 device types. The FDA files 51 510(k) clearances under its listings, the newest dated April 9, 2026. 3 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2023950
- Address
- 2875 Loker Avenue East, Carlsbad, CA, United States, 92010
- Owner or operator
- Zest Anchors, LLC (2023950)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 2, 1992
- Registered through
- 2026
- Brand names listed
- R-Tx Abutments
Devices it lists
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 |
| September 2, 2020 | K200827 | LOCATOR R-Tx | NHA | Substantially Equivalent | Ivory Super Holdco, Incp. | accessdata.fda.gov |
| September 11, 2019 | K191619 | TurboTemp EZ | EBG | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| March 4, 2016 | K151789 | LOCATOR F-Tx Attachment System | NHA | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| November 23, 2015 | K152349 | Star+ VPS Scannable Impression Material | ELW | Substantially Equivalent | Danville Materials, LLC | accessdata.fda.gov |
| August 28, 2015 | K151088 | DMRC Bulk Fill | EBF | Substantially Equivalent | Danville Materials, LLC | accessdata.fda.gov |
| July 24, 2015 | K150295 | LOCATOR RTx | NHA | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| March 18, 2015 | K142886 | DMRC Self-Cure Bracket Adhesive One Step and Primer | DYH | Substantially Equivalent | Danville Materials, LLC | accessdata.fda.gov |
| February 13, 2015 | K142881 | DMRC Dual Cure Orthodontic Band Cement | DYH | Substantially Equivalent | Danville Materials, LLC | accessdata.fda.gov |
| June 25, 2014 | K133327 | SATURNO(TM) OVERDENTURE IMPLANT SYSTEM | DZE | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| June 16, 2014 | K140570 | CHAIRSIDE ATTACHMENT PROCESSING MATERIAL | EBI | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| September 25, 2012 | K121880 | DMRC NANOFLOW DMRC NANOCOMPOSITE EBOND SURE ETCH GEL SURE ETCH LIQUID | EBF | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| June 6, 2012 | K120198 | LOCATOR OVERDENTURE IMPLANT SYSTEM | DZE | Substantially Equivalent | Zest Anchors, LLC | accessdata.fda.gov |
| October 28, 2011 | K112445 | SOFRELINER TOUGH S | EBI | Substantially Equivalent | Tokuyama Dental Corporation | accessdata.fda.gov |
| September 21, 2011 | K111876 | Z BOND, PRELUDE ONE | KLE | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| May 27, 2011 | K110642 | SILJETR SYSTEM | EBF | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| February 4, 2011 | K102753 | TURBO TEMP 3 | EBG | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| December 16, 2009 | K092912 | STARFILL 2B HV (HIGH VISCOSITY) ROCKCORE, MODEL: 90838 AND STARFILL 2B LV (LOW VISCOSITY), MODEL: 90150 | EBF | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| September 16, 2009 | K092319 | STAR VPS, MODEL 80014-01, FIRST QUATER, MODEL 90649, FIRST HALF, MODEL 89387 | ELW | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| March 31, 2009 | K090106 | PRELUDE ONE | KLE | Substantially Equivalent | Danville Materials, Inc. | 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 |
| June 29, 2004 | K040952 | PRELUDE | KLE | Substantially Equivalent | Danville Materials, 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 |
| January 9, 2004 | K033215 | PREPAIR | KOJ | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| May 3, 2002 | K020760 | STARFLOW HV | EBF | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| October 10, 2001 | K012354 | SNOWPOST, SNOWLIGHT | ELR | Substantially Equivalent | Danville Materials, Inc. | accessdata.fda.gov |
| September 28, 2001 | K012911 | 3I LOCATER ABUTMENT SYSTEM | DZE | Substantially Equivalent | Implant Innovations, Inc. | accessdata.fda.gov |
| November 8, 2000 | K002502 | CERAM-PRIME | KLE | Substantially Equivalent | S & C Polymer GmbH | accessdata.fda.gov |
| March 17, 2000 | K994257 | LOCATOR IMPLANT ANCHOR | DZE | Substantially Equivalent | Zest Anchors, Inc. | accessdata.fda.gov |
| July 9, 1999 | K991450 | ETCHING GEL | EBF | Substantially Equivalent | Silicon-Und Composite Spezialitaten GmbH | accessdata.fda.gov |
| June 3, 1999 | K991442 | LC MICROFILL | EBF | Substantially Equivalent | S & C Polymer GmbH | accessdata.fda.gov |
| March 9, 1999 | K990108 | LC FLOWFILL | EBF | Substantially Equivalent | S & C Polymer GmbH | accessdata.fda.gov |
| September 15, 1998 | K982480 | PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. | EIA | Substantially Equivalent | Dentalview, Inc. | accessdata.fda.gov |
| October 21, 1997 | K973492 | DENTALVIEW PERIOVIEW SYSTEM | EIA | Substantially Equivalent | Dentalview, Inc. | accessdata.fda.gov |
| September 17, 1997 | K970589 | MICROETCHER AP | KOJ | Substantially Equivalent | Danville Engineering, Inc. | accessdata.fda.gov |
| February 8, 1996 | K955445 | CARIES FINDER | LFC | Substantially Equivalent | Danville Engineering, Inc. | accessdata.fda.gov |
| October 3, 1995 | K953504 | MICROPRIME | KLE | Substantially Equivalent | Danville Engineering, Inc. | accessdata.fda.gov |
| March 31, 1995 | K951075 | S & C VINYL POLYSILOXANE IMPRESSION MATERIAL | ELW | Substantially Equivalent | S & C Polymer GmbH | 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 |
| November 20, 1990 | K902836 | MICROETCHER | KOJ | Substantially Equivalent | Danville Engineering, Inc. | accessdata.fda.gov |
| July 15, 1988 | K882576 | ACID ETCH GEL | EBF | Substantially Equivalent | Pulpdent Corp. of America | accessdata.fda.gov |
| July 6, 1979 | K790788 | FISSURE SEALER AND BONDING AGENT | EBC | Substantially Equivalent | Scientific Pharmaceuticals, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| November 22, 2019 | 85369 | Class II | Ongoing | LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1. | 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. | accessdata.fda.gov |
| January 16, 2014 | 67315 | Class II | Terminated | 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 | 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 o | accessdata.fda.gov |
| April 9, 2008 | 48645 | Not yet classified | Terminated | "LOCATOR Abutment for 5.7 Screw-Vent & Compatibles." Zest Anchors, Inc. Product is sold for use with any Zimmer Dental 5.7 mm diameter Tapered Screw-Vent Implant. The product is used with supra-gingival, universal hinge, | 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 o | accessdata.fda.gov |
Compare with other makers
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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.