LOCATOR Overdenture Implant System

FDA UDI

Class II (US FDA UDI)

by Zest Anchors, LLC

Identity

Trade Name: LOCATOR Overdenture Implant System FDA UDI
Generic Name: Screw endosteal dental implant, two-piece FDA UDI
Device Name: LOCATOR Overdenture Implant, 3.9mmD x 14mmL, 5mm Cuff FDA UDI
Model / Reference: 07508-05 FDA UDI
Description: LOCATOR Overdenture Implant, 3.9mmD x 14mmL, 5mm Cuff FDA UDI

Identifiers

Primary DI / UDI-DI: 00840481131141 FDA UDI
FDA Product Code: DZE FDA UDI
GMDN Term: Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3640 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 5 Millimeter FDA UDI

Category: Screw endosteal dental implant, two-piece

The LOCATOR Overdenture Implant System is a two-piece, alloplastic screw endosteal dental implant designed to provide support and retention for dental prostheses. Made from titanium or other biocompatible materials, it features a threaded screw anchor and a retrievable abutment. The device is intended for single-tooth or overdenture applications.

Similar devices

Also classified as Screw endosteal dental implant, two-piece.

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LW Vis Abutment — Ossvis Co., Ltd. · Class II
s-Clean TiN Half Coating Angled Abutment — DENTIS CO. , LTD · Class II
ET II Fixture SA Mini No-Mounted — HIOSSEN INC. · Class II
LW Vis Abutment — Ossvis Co., Ltd. · Class II
PRAMA RF WHITE IMPLANT ZIRTI — SWEDEN & MARTINA INC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Zest Anchors, LLC

Sources (1)

FDA UDI d446daf9-8c7c-4a1e-9d34-dc37e8c481b4 35 fields · synced Jul 29, 2026