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Zest 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: linkedin.com/company/zest-anchors
Facebook: facebook.com/ZestDentalSolutions
Email: [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 69 of 70

Device	Model / Reference	Registries	Class	Status
LOCATOR Fixed	09508	FDA UDI	Class II	Active
LOCATOR, Dentsply Sirona System	30700-05	FDA UDI	Class II	Active
Zaag	04352	FDA UDI	Class I	Active
LOCATOR, compatible with AstraTech Implant System	02795	FDA UDI	Class II	Active
LOCATOR, compatible with Anthogyr System	08393	FDA UDI	Class I	Active
LOCATOR, Dentsply Sirona System	30700-06	FDA UDI	Class II	Active
LOCATOR, Dentsply Sirona System	30702-01	FDA UDI	Class II	Active
Znano	90-00142	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00139	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00143	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00141	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00114	EUDAMEDFDA UDI	Class IIa	Active
Locator Overdenture Implant System	K120198	FDA 510(k)	Class II	Active
Saturno(tm) Overdenture Implant System	K133327	FDA 510(k)	Class II	Active
LOCATOR® Angled Abutment	K260555	FDA 510(k)	Class II	Active
Zest Implant Anchor Advanced Generation (dental)	K934668	FDA 510(k)	Class II	Active
LOCATOR® Angled Abutment	K250721	FDA 510(k)	Class II	Active
Zest Mark Ii (standard & Mini)	K861561	FDA 510(k)	Class I	Active
Bioceram Zest Plant	K840244	FDA 510(k)	Class II	Active
Locator Implant Anchor	K994257	FDA 510(k)	Class II	Active
Chairside Attachment Processing Material	K140570	FDA 510(k)	Class II	Active
LOCATOR Angled Abutment	K243272	FDA 510(k)	Class II	Active
Magne-Dent Magnet/Zest Retrofit Keeper	K882063	FDA 510(k)	Class I	Active
Locator Implant Anchor Attachment System	K083324	FDA 510(k)	Class II	Active
Modification To: Locator Implant Anchor	K072878	FDA 510(k)	Class II	Active
LOCATOR Angled Abutment (Various)	K233587	FDA 510(k)	Class II	Active
Zest Anchor Advanced Generation	K925700	FDA 510(k)	Class I	Active
X-2 Implant Abutment; Bar Male; Distal Extension Male	K042466	FDA 510(k)	Class II	Active
Zest Plant	K801524	FDA 510(k)	Class II	Active
High Retention Attachment System	K213391	FDA 510(k)	Class II	Active
High Retention Attachment System	K220252	FDA 510(k)	Class II	Active
Zest Endodontic Stabilizer	K801525	FDA 510(k)	Class II	Active
TurboTemp EZ	K191619	FDA 510(k)	Class II	Active
LOCATOR F-Tx Attachment System	K151789	FDA 510(k)	Class II	Active
Locator Bar Female, Locator Laser Bar Female, Locator Bar Cast-To Female, Models 08587, 08588, 08586	K033699	FDA 510(k)	Class II	Active
LOCATOR® Angled Abutment	K252944	FDA 510(k)	Class II	Active
Zest Implant Anchor	K925849	FDA 510(k)	Class II	Active
Znano	90-00113	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00146	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00116	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00122	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00118	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00115	EUDAMEDFDA UDI	Class IIa	Active
Locator	09260-4	EUDAMEDFDA UDI	Class I	Active
Locator R-Tx	30060-01-2	EUDAMEDFDA UDI	Class I	Active
Znano	90-00137	EUDAMEDFDA UDI	Class IIa	Active
Znano	90-00112	EUDAMEDFDA UDI	Class IIa	Active
Locator R-Tx	30060-01-4	EUDAMEDFDA UDI	Class I	Active
Znano	90-00119	EUDAMEDFDA UDI	Class IIa	Active
Locator	09260-10	EUDAMEDFDA UDI	Class I	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