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Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Dental precision attachment fitting/adjustment tool FDA UDI
Device Name
TWO PIECE TREPHINE REMOVAL TOOL LONG 31.8MM TL THREADED FDA UDI
Model / Reference
04941202 FDA UDI
Description
TWO PIECE TREPHINE REMOVAL TOOL LONG 31.8MM TL THREADED FDA UDI

Identifiers

Catalog Number
04941202 FDA UDI
Primary DI / UDI-DI
00614950029969 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Dental precision attachment fitting/adjustment tool FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental precision attachment fitting/adjustment tool

Ace by Ace Surgical Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental precision attachment fitting/adjustment tool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e14b6c6-4222-47a8-99ea-67710b093aa5 35 fields · synced Jun 1, 2026