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Foundation® Hip System

FDA UDI

Class II (US FDA UDI)

by Encore Medical, L.p.

Identity

Trade Name
FOUNDATION® HIP SYSTEM FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
Foundation PS Femur, NonPorous, TiNbN Coated, Sz 7 RT FDA UDI
Model / Reference
214-09-007 FDA UDI
Description
Foundation PS Femur, NonPorous, TiNbN Coated, Sz 7 RT FDA UDI

Identifiers

Primary DI / UDI-DI
00888912110662 FDA UDI
510(k) Number
K122239 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 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

Yes

FDA UDI

Category: Coated hip femur prosthesis, modular

Foundation® Hip System by Encore Medical, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated hip femur prosthesis, modular.

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 4a93784e-82d8-476f-88c4-2638c873ffde 34 fields · synced May 29, 2026