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LOCATOR, compatible with AstraTech Implant System

FDA UDI

Class I (US FDA UDI)

by Zest Anchors, LLC

Identity

Trade Name
LOCATOR, compatible with AstraTech Implant System FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
LOCATOR Replacement Male (CLEAR) (4 Pack) FDA UDI
Model / Reference
08524 FDA UDI
Description
LOCATOR Replacement Male (CLEAR) (4 Pack) FDA UDI

Identifiers

Catalog Number
08524-AT-SB FDA UDI
Primary DI / UDI-DI
00840481126611 FDA UDI
FDA Product Code
EGG FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3165 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Category: Dental implant suprastructure, permanent, preformed

LOCATOR, compatible with AstraTech Implant System by Zest Anchors, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zest Anchors, LLC

Sources (1)

  • FDA UDI 0ee04513-d6da-4c80-86eb-da2b8d8ab9d6 35 fields · synced Jun 9, 2026