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Integra® First Choice®

FDA UDI

Class II (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Integra® First Choice® FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
The Modular Ulnar Head Head Trial is used to determine the proper implant head size by evaluating congurency and joint articulation. FDA UDI
Model / Reference
TRL600H175 FDA UDI
Description
The Modular Ulnar Head Head Trial is used to determine the proper implant head size by evaluating congurency and joint articulation. FDA UDI

Identifiers

Catalog Number
TRL-600-H175 FDA UDI
Primary DI / UDI-DI
10381780236726 FDA UDI
510(k) Number
K112481 FDA UDI
FDA Product Code
KXE FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3810 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

No

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: Surgical implant template, reusable

Integra® First Choice® by Ascension Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI acf5b6b4-d9da-4d55-a310-b5ae6a2e0160 38 fields · synced Jun 8, 2026