Locator

FDA UDI

Class I (US FDA UDI)

by Zest Anchors, LLC

Identity

Trade Name: LOCATOR FDA UDI
Generic Name: Fluted surgical drill bit, reusable FDA UDI
Device Name: Guided Cortical Drill 3.3mm FDA UDI
Model / Reference: 07986 FDA UDI
Description: Guided Cortical Drill 3.3mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00840481130526 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Fluted surgical drill bit, 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

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Fluted surgical drill bit, reusable

Locator by Zest Anchors, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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ROTACYJNE NARZĘDZIA CHIRURGICZNE — ChM spółka z ograniczoną odpowiedzialnością · Class IIa
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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 I	Pending data

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Manufacturer

Manufacturer: Zest Anchors, LLC

Sources (1)

FDA UDI 1bc924f7-82a8-4aec-b046-94460afd6304 34 fields · synced Jun 9, 2026