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OMNI K2 Hip

FDA UDI

Class II (US FDA UDI)

by OMNIlife science, Inc.

Identity

Trade Name
OMNI K2 Hip FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
K2 Mid Length Stem Size 11 FDA UDI
Model / Reference
HC-30110 FDA UDI
Description
K2 Mid Length Stem Size 11 FDA UDI

Identifiers

Catalog Number
HC-30110 FDA UDI
Primary DI / UDI-DI
00841690118497 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Coated hip femur prosthesis, modular

OMNI K2 Hip by OMNIlife science, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated hip femur prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aa326044-589a-4702-8ff6-1c5e915b9c09 35 fields · synced Jun 9, 2026