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Balance Hip System

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
BALANCE HIP SYSTEM FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Model / Reference
180000 FDA UDI

Identifiers

Catalog Number
180000 FDA UDI
Primary DI / UDI-DI
00880304268500 FDA UDI
510(k) Number
K030055 FDA UDI
K050251 FDA UDI
K921224 FDA UDI
FDA Product Code
JDI FDA UDI
KWZ FDA UDI
KWY FDA UDI
LPH FDA UDI
LZY FDA UDI
MEH FDA UDI
LZO FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3310 FDA UDI
888.3390 FDA UDI
888.3358 FDA UDI
888.3360 FDA UDI
888.3353 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: Coated hip femur prosthesis, modular

Balance Hip System by Biomet Orthopedics, Inc. — 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 58e26aaa-4b94-48c9-b761-172b4cc8050d 36 fields · synced May 30, 2026