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Cut Guide

FDA UDI

Class I (US FDA UDI)

by Treace Medical Concepts, Inc.

Identity

Trade Name
Cut Guide FDA UDI
Generic Name
Osteotomy guide, reusable FDA UDI
Device Name
lesser TMT cut guide small FDA UDI
Model / Reference
1405-2541 FDA UDI
Description
lesser TMT cut guide small FDA UDI

Identifiers

Primary DI / UDI-DI
00810111220316 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Osteotomy guide, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Osteotomy guide, reusable

Cut Guide by Treace Medical Concepts, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Osteotomy guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6fd5ec46-623c-4336-9aeb-a010cb6e74fa 33 fields · synced May 31, 2026