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BKS® Uni

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name
BKS® Uni FDA UDI
Generic Name
Uncoated knee femur prosthesis, metallic FDA UDI
Device Name
Femoral Component Medial Nonporous Size 8 Left FDA UDI
Model / Reference
761-1801 FDA UDI
Description
Femoral Component Medial Nonporous Size 8 Left FDA UDI

Identifiers

Primary DI / UDI-DI
00822409109272 FDA UDI
510(k) Number
K211471 FDA UDI
FDA Product Code
HSX FDA UDI
GMDN Term
Uncoated knee femur prosthesis, metallic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3520 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: Uncoated knee femur prosthesis, metallic

BKS® Uni by Ortho Development Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uncoated knee femur prosthesis, metallic.

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 1861b54c-b772-4871-82f4-ca0f0d42b5ee 35 fields · synced May 30, 2026