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Kosmo Femoral Hip System

FDA UDI

Class II (US FDA UDI)

by b-ONE Ortho Corp.

Identity

Trade Name
Kosmo Femoral Hip System FDA UDI
Generic Name
Uncoated hip femur prosthesis, modular FDA UDI
Device Name
Proportional Offset Collarless Hip Stem 132°, Size 4, For Cemented Use Only FDA UDI
Model / Reference
8810422235 FDA UDI
Description
Proportional Offset Collarless Hip Stem 132°, Size 4, For Cemented Use Only FDA UDI

Identifiers

Catalog Number
8810422235 FDA UDI
Primary DI / UDI-DI
00843575120922 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
JDI FDA UDI
GMDN Term
Uncoated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Uncoated hip femur prosthesis, modular

Kosmo Femoral Hip System by b-ONE Ortho Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated hip femur prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
b-ONE Ortho Corp.

Sources (1)

  • FDA UDI 4acaa8b8-b050-4990-b831-c961cf0bee8b 34 fields · synced Jun 6, 2026