← Back to catalogue

BKS® Uni

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name
BKS® Uni FDA UDI
Generic Name
Uncoated knee tibia prosthesis, metallic FDA UDI
Device Name
Tibial Tray Medial Nonporous Size 5 Left FDA UDI
Model / Reference
762-5100 FDA UDI
Description
Tibial Tray Medial Nonporous Size 5 Left FDA UDI

Identifiers

Primary DI / UDI-DI
00822409109371 FDA UDI
510(k) Number
K211471 FDA UDI
FDA Product Code
HSX FDA UDI
GMDN Term
Uncoated knee tibia 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 tibia 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 tibia prosthesis, metallic.

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 72b4e75b-c248-4f98-ae18-04e660823c46 35 fields · synced May 30, 2026