← Back to catalogue

LOCATOR, compatible with Implant Direct

FDA UDI

Class I (US FDA UDI)

by Zest Anchors, LLC

Identity

Trade Name
LOCATOR, compatible with Implant Direct FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
LOCATOR Angle Measurement Guide FDA UDI
Model / Reference
09530 FDA UDI
Description
LOCATOR Angle Measurement Guide FDA UDI

Identifiers

Catalog Number
09530-ID-SB FDA UDI
Primary DI / UDI-DI
00840481134050 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation depth/angle gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implantation depth/angle gauge, reusable

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

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Zest Anchors, LLC

Sources (1)

  • FDA UDI 2c21a95f-878a-4d65-b981-53624fcf5abc 35 fields · synced Jun 9, 2026