Manufacturer registered with FDA
Zest Anchors, LLC
Carlsbad, CA, United States. Lists 29 dental device types with FDA across 3 registered establishments, and holds 26 510(k) clearances as applicant.
- Device types listed
- 29
- Brands and models
- 1
- 510(k) clearances
- 261980–2026
- Markets registered in
- 13444 registrations outside the US
- Establishments
- 3United States
510(k) clearances per year, 1980–2026
Registered in 13 markets
Where regulators' registries name Zest Anchors, LLC as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Zest Anchors, LLC | 26 clearances | 1980–2026 | Below |
| Canada | Health Canada | Registration holder | ZEST ANCHORS, LLC | 146 | 2002–2026 | Pure Global AI |
| United Kingdom | MHRA | Manufacturer | Zest Anchors, LLC | 92 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | Zest Anchors, LLCZest Anchors, Inc. · Zest Anchors, Inc · +2 | 62 | 2000–2026 | Pure Global AI |
| European Union | EUDAMED | Manufacturer | Zest Anchors, LLC | 42 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | ZEST ANCHORS, LLCZEST ANCHORS LLC · ZEST ANCHORS, INC. · +1 | 25 | 2006–2023 | Pure Global AI |
| Australia | TGA | Manufacturer | Zest Anchors LLC | 18 | 2016–2026 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | ZEST ANCHORS LLCZEST ANCHORS, LLC., | 17 | — | Pure Global AI |
| Costa Rica | Ministerio de Salud | Manufacturer | Zest Anchors LLCDANVILLE MATERIALS RESEARCH CENTER · ZEST ANCHORS | 15 | — | Pure Global AI |
| Israel | AMAR | Manufacturer | Zest Anchors, LLCZest Anchors LLC · Zest Anchors, Inc. · +1 | 14 | — | Pure Global AI |
| China | NMPA | Registration holder | 泽斯安科有限责任公司Zest Anchors, LLC | 5 | — | Pure Global AI |
| Saudi Arabia | SFDA | Manufacturer | ZEST ANCHORS LLC | 5 | — | Pure Global AI |
| Hong Kong | MDD | Manufacturer | Zest Anchors, LLC | 3 | 2025–2026 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Zest Anchors, LLC currently lists, by FDA device type, with the brand and model names on the listing.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names Zest Anchors, LLC as the applicant, including filings under its other names.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 9 Apr 2026 | K260555 | LOCATOR® Angled Abutment | NHA Endosseous Dental Implant Abutment |
| 15 Oct 2025 | K252944 | LOCATOR® Angled Abutment | NHA Endosseous Dental Implant Abutment |
| 20 Aug 2025 | K250721 | LOCATOR® Angled Abutment | NHA Endosseous Dental Implant Abutment |
| 14 Jan 2025 | K243272 | LOCATOR Angled Abutment | NHA Endosseous Dental Implant Abutment |
| 3 Jun 2024 | K233587 | LOCATOR Angled Abutment (Various) | NHA Endosseous Dental Implant Abutment |
| 14 Apr 2022 | K220252 | High Retention Attachment System | NHA Endosseous Dental Implant Abutment |
| 11 Jan 2022 | K213391 | High Retention Attachment System | NHA Endosseous Dental Implant Abutment |
| 11 Sep 2019 | K191619 | TurboTemp EZ | EBG Resin Temporary Crown and Bridge |
| 4 Mar 2016 | K151789 | LOCATOR F-Tx Attachment System | NHA Endosseous Dental Implant Abutment |
| 24 Jul 2015 | K150295 | LOCATOR RTx | NHA Endosseous Dental Implant Abutment |
| 25 Jun 2014 | K133327 | SATURNO(TM) OVERDENTURE IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 16 Jun 2014 | K140570 | CHAIRSIDE ATTACHMENT PROCESSING MATERIAL | EBI Rebasing Repairing Relining Denture Resin |
| 6 Jun 2012 | K120198 | LOCATOR OVERDENTURE IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 25 Feb 2009 | K083324 | LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM | NHA Endosseous Dental Implant Abutment |
| 3 Dec 2007 | K072878 | MODIFICATION TO: LOCATOR IMPLANT ANCHOR | NHA Endosseous Dental Implant Abutment |
| 24 Nov 2004 | K042466 | X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE | NHA Endosseous Dental Implant Abutment |
| 22 Apr 2004 | K033699 | LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586 | DZE Root-Form Endosseous Implant |
| 17 Mar 2000 | K994257 | LOCATOR IMPLANT ANCHOR | DZE Root-Form Endosseous Implant |
| 18 Nov 1994 | K925849 | ZEST IMPLANT ANCHOR | DZE Root-Form Endosseous Implant |
| 22 Jun 1994 | K934668 | ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL) | DZE Root-Form Endosseous Implant |
| 7 Apr 1994 | K925700 | ZEST ANCHOR ADVANCED GENERATION | EGG All Precision Attachment |
| 13 Jun 1988 | K882063 | MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER | EGG All Precision Attachment |
| 21 May 1986 | K861561 | ZEST MARK II (STANDARD & MINI) | EGG All Precision Attachment |
| 1 May 1984 | K840244 | BIOCERAM ZEST PLANT | DZE Root-Form Endosseous Implant |
| 21 Jul 1980 | K801525 | ZEST ENDODONTIC STABILIZER | ELS Endodontic Stabilizing Splint |
| 21 Jul 1980 | K801524 | ZEST PLANT | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: Nobel Biocare Services AG (3), ZimVie US Corp LLC (2), SIC invent AG (2), Digital Age Dental Laboratories, Ltd. (1), Paltop Advanced Dental Solutions Inc. (1), Neoss AB (1).
Also lists devices cleared under other names
Zest Anchors, LLC lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Danville Materials, LLC (15), S & C Polymer GmbH (4), Danville Engineering, Inc. (4), Dentalview, Inc. (2), Ivory Super Holdco Inc. / Zest Anchors, LLC (1), Ivory Super Holdco, Incp. (1), Tokuyama Dental Corporation (1), Implant Innovations, Inc. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 15 Apr 2021 | K203701 | Locator Overdenture Implant System | Ivory Super Holdco Inc. / Zest Anchors, LLC | DZE Root-Form Endosseous Implant |
| 2 Sep 2020 | K200827 | LOCATOR R-Tx | Ivory Super Holdco, Incp. | NHA Endosseous Dental Implant Abutment |
| 23 Nov 2015 | K152349 | Star+ VPS Scannable Impression Material | Danville Materials, LLC | ELW Impression Material |
| 28 Aug 2015 | K151088 | DMRC Bulk Fill | Danville Materials, LLC | EBF Resin Tooth Shade Material |
| 18 Mar 2015 | K142886 | DMRC Self-Cure Bracket Adhesive One Step and Primer | Danville Materials, LLC | DYH Resin Bracket and Tooth Conditioner Adhesive |
| 13 Feb 2015 | K142881 | DMRC Dual Cure Orthodontic Band Cement | Danville Materials, LLC | DYH Resin Bracket and Tooth Conditioner Adhesive |
| 25 Sep 2012 | K121880 | DMRC NANOFLOW DMRC NANOCOMPOSITE EBOND SURE ETCH GEL SURE ETCH LIQUID | Danville Materials, LLC | EBF Resin Tooth Shade Material |
| 28 Oct 2011 | K112445 | SOFRELINER TOUGH S | Tokuyama Dental Corporation | EBI Rebasing Repairing Relining Denture Resin |
| 21 Sep 2011 | K111876 | Z BOND, PRELUDE ONE | Danville Materials, LLC | KLE Resin Tooth Bonding Agent |
| 27 May 2011 | K110642 | SILJETR SYSTEM | Danville Materials, LLC | EBF Resin Tooth Shade Material |
| 4 Feb 2011 | K102753 | TURBO TEMP 3 | Danville Materials, LLC | EBG Resin Temporary Crown and Bridge |
| 16 Dec 2009 | K092912 | STARFILL 2B HV (HIGH VISCOSITY) ROCKCORE, MODEL: 90838 AND STARFILL 2B LV (LOW VISCOSITY), MODEL: 90150 | Danville Materials, LLC | EBF Resin Tooth Shade Material |
| 16 Sep 2009 | K092319 | STAR VPS, MODEL 80014-01, FIRST QUATER, MODEL 90649, FIRST HALF, MODEL 89387 | Danville Materials, LLC | ELW Impression Material |
| 31 Mar 2009 | K090106 | PRELUDE ONE | Danville Materials, LLC | KLE Resin Tooth Bonding Agent |
| 29 Jun 2004 | K040952 | PRELUDE | Danville Materials, LLC | KLE Resin Tooth Bonding Agent |
| 9 Jan 2004 | K033215 | PREPAIR | Danville Materials, LLC | KOJ Airbrush |
| 3 May 2002 | K020760 | STARFLOW HV | Danville Materials, LLC | EBF Resin Tooth Shade Material |
| 10 Oct 2001 | K012354 | SNOWPOST, SNOWLIGHT | Danville Materials, LLC | ELR Root Canal Post |
| 28 Sep 2001 | K012911 | 3I LOCATER ABUTMENT SYSTEM | Implant Innovations, Inc. | DZE Root-Form Endosseous Implant |
| 8 Nov 2000 | K002502 | CERAM-PRIME | S & C Polymer GmbH | KLE Resin Tooth Bonding Agent |
| 9 Jul 1999 | K991450 | ETCHING GEL | Silicon-Und Composite Spezialitaten GmbH | EBF Resin Tooth Shade Material |
| 3 Jun 1999 | K991442 | LC MICROFILL | S & C Polymer GmbH | EBF Resin Tooth Shade Material |
| 9 Mar 1999 | K990108 | LC FLOWFILL | S & C Polymer GmbH | EBF Resin Tooth Shade Material |
| 15 Sep 1998 | K982480 | PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. | Dentalview, Inc. | EIA Operative Dental Unit |
| 21 Oct 1997 | K973492 | DENTALVIEW PERIOVIEW SYSTEM | Dentalview, Inc. | EIA Operative Dental Unit |
| 17 Sep 1997 | K970589 | MICROETCHER AP | Danville Engineering, Inc. | KOJ Airbrush |
| 8 Feb 1996 | K955445 | CARIES FINDER | Danville Engineering, Inc. | LFC Caries Detection Device |
| 3 Oct 1995 | K953504 | MICROPRIME | Danville Engineering, Inc. | KLE Resin Tooth Bonding Agent |
| 31 Mar 1995 | K951075 | S & C VINYL POLYSILOXANE IMPRESSION MATERIAL | S & C Polymer GmbH | ELW Impression Material |
| 20 Nov 1990 | K902836 | MICROETCHER | Danville Engineering, Inc. | KOJ Airbrush |
| 15 Jul 1988 | K882576 | ACID ETCH GEL | Pulpdent Corp. of America | EBF Resin Tooth Shade Material |
| 6 Jul 1979 | K790788 | FISSURE SEALER AND BONDING AGENT | Scientific Pharmaceuticals | EBC Pit and Fissure Sealant and Conditioner |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| Danville Materials Research CenterFDA reg. 3010664129 | Anaheim, CA, United States | Manufacturer, Repacker / relabeler |
| ZEST ANCHORS, LLCFDA reg. 3006796211 | Escondido, CA, United States | Manufacturer |
| ZEST ANCHORS, LLCFDA reg. 2023950 | Carlsbad, CA, United States | Manufacturer, Repacker / relabeler, Specification developer |
Other names on FDA records
Danville Materials Research Center
Sources
FDA establishment registration & device listing (search FDA, owner/operator 2023950). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.