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Omnifit

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name
Omnifit FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
Hip Stem FDA UDI
Model / Reference
6076-0525A FDA UDI
Description
Hip Stem FDA UDI

Identifiers

Catalog Number
6076-0525A FDA UDI
Primary DI / UDI-DI
07613327023527 FDA UDI
510(k) Number
K031744 FDA UDI
FDA Product Code
LWJ FDA UDI
JDI FDA UDI
KWL FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3360 FDA UDI
888.3350 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Press-fit femoral stem prosthesis

Omnifit by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit femoral stem prosthesis.

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 3796d661-9f0a-41ed-a4c8-10cbe73f7f91 36 fields · synced Jun 1, 2026