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BIOLOX® Delta Hip System

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
BIOLOX® Delta Hip System FDA UDI
Generic Name
Ceramic femoral head prosthesis FDA UDI
Model / Reference
12-115109 FDA UDI

Identifiers

Catalog Number
12-115109 FDA UDI
Primary DI / UDI-DI
00887868248405 FDA UDI
510(k) Number
K042091 FDA UDI
K051411 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Ceramic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Ceramic femoral head prosthesis

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

Similar devices

Also classified as Ceramic femoral head prosthesis.

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 e86f2767-41e8-4cca-bebd-153ab7de6cec 36 fields · synced Jun 8, 2026