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OsteoGen Strip - Small

FDA UDI

Class II (US FDA UDI)

by Impladent

Identity

Trade Name
OsteoGen Strip - Small FDA UDI
Generic Name
Composite bone graft FDA UDI
Device Name
OsteoGen Strips. OsteoGen bone graft combined with a bovine achilles tendon carrier FDA UDI
Model / Reference
OSS12203 FDA UDI
Description
OsteoGen Strips. OsteoGen bone graft combined with a bovine achilles tendon carrier FDA UDI

Identifiers

Primary DI / UDI-DI
00855286006273 FDA UDI
510(k) Number
K090794 FDA UDI
FDA Product Code
NPM FDA UDI
GMDN Term
Composite bone graft FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 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

No

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: Composite bone graft

OsteoGen Strip - Small by Impladent — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Composite bone graft.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Impladent

Sources (1)

  • FDA UDI b859a9fe-ece9-4a22-a4ce-c9e2379b621c 34 fields · synced Jun 8, 2026