← Back to catalogue

Biomet Hip System

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
BIOMET HIP SYSTEM FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Model / Reference
163665 FDA UDI

Identifiers

Catalog Number
163665 FDA UDI
Primary DI / UDI-DI
05019279400751 FDA UDI
510(k) Number
K911684 FDA UDI
K942479 FDA UDI
K953925 FDA UDI
K974558 FDA UDI
FDA Product Code
JDI FDA UDI
LZO FDA UDI
KRO FDA UDI
JDG FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3353 FDA UDI
888.3510 FDA UDI
888.3360 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: Metallic femoral head prosthesis

Biomet Hip System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a1447e63-c9eb-49bf-ab84-434cfd69cfbc 36 fields · synced Jun 8, 2026