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Integra®Ti6®

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Integra®Ti6® FDA UDI
Generic Name
Surgical implant handling forceps FDA UDI
Device Name
The Bone Reduction Forceps are used to hold objects in the Integra Ti6 system. These forceps have a sweetheart style. FDA UDI
Model / Reference
FS1010 FDA UDI
Description
The Bone Reduction Forceps are used to hold objects in the Integra Ti6 system. These forceps have a sweetheart style. FDA UDI

Identifiers

Catalog Number
FS1010 FDA UDI
Primary DI / UDI-DI
10381780244912 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant handling forceps

Integra®Ti6® 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 5cc98b60-3fa7-4979-9bd1-a484323976e1 37 fields · synced Jun 8, 2026