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Integra®

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Integra® FDA UDI
Generic Name
Surgical implant handling forceps FDA UDI
Device Name
Integra®Total Foot System The k-wire distraction/compression forceps are used to hold k-wire in the Integra Total Foot System. FDA UDI
Model / Reference
KDFTFS00 FDA UDI
Description
Integra®Total Foot System The k-wire distraction/compression forceps are used to hold k-wire in the Integra Total Foot System. FDA UDI

Identifiers

Catalog Number
KDF-TFS-00 FDA UDI
Primary DI / UDI-DI
10381780245872 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Surgical implant handling forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant handling forceps

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

Similar devices

Also classified as Surgical implant handling forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ascension Orthopedics, Inc.

Sources (1)

  • FDA UDI 25a2b380-f851-41e5-a70a-f12183fbeed9 37 fields · synced Jun 8, 2026