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Locator

FDA UDI

Class I (US FDA UDI)

by Zest Anchors, LLC

Identity

Trade Name
LOCATOR FDA UDI
Generic Name
Dental soft-tissue coring punch, reusable FDA UDI
Device Name
SNDI Tissue Punch Assembly, 5.0 mmD FDA UDI
Model / Reference
07642 FDA UDI
Description
SNDI Tissue Punch Assembly, 5.0 mmD FDA UDI

Identifiers

Primary DI / UDI-DI
00840481109683 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental soft-tissue coring punch, 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental soft-tissue coring punch, reusable

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

Similar devices

Also classified as Dental soft-tissue coring punch, reusable.

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 ffc95dd1-4035-4fd7-89f6-c0444712dbab 34 fields · synced Jun 9, 2026