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Collage

FDA UDI

Class II (US FDA UDI)

by Orthofix US LLC

Identity

Trade Name
Collage FDA UDI
Generic Name
Bone matrix implant, composite FDA UDI
Device Name
Collage Osteoconductive Scaffold Putty, 5cc FDA UDI
Model / Reference
710005 FDA UDI
Description
Collage Osteoconductive Scaffold Putty, 5cc FDA UDI

Identifiers

Primary DI / UDI-DI
18257200115112 FDA UDI
510(k) Number
K062353 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone matrix implant, composite FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone matrix implant, composite

Collage by Orthofix US LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, composite.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix US LLC

Sources (1)

  • FDA UDI 26bce942-1488-4ccb-9f1e-51eccc632d6a 36 fields · synced Jun 8, 2026