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Biolox Delta

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name
Biolox Delta FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Device Name
32mm +2 FDA UDI
Model / Reference
136-3203 FDA UDI
Description
32mm +2 FDA UDI

Identifiers

Primary DI / UDI-DI
00822409015726 FDA UDI
510(k) Number
K111936 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Coated hip femur prosthesis, modular 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

Dimensions & Sizes

Size
Outer Diameter — 32 Millimeter FDA UDI
Length — 2 Millimeter FDA UDI

Category: Coated hip femur prosthesis, modular

Biolox Delta by Ortho Development Corp. — 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 3e6dfa84-5da6-4c58-9839-e771d0a56f39 36 fields · synced Jun 1, 2026