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Uni Tibial Tray

FDA UDI

Class II (US FDA UDI)

by Signal Medical Corp.

Identity

Trade Name
Uni Tibial Tray FDA UDI
Generic Name
Coated unicondylar knee tibia prosthesis FDA UDI
Device Name
Uni Tibial Tray Size 3 FDA UDI
Model / Reference
3 FDA UDI
Description
Uni Tibial Tray Size 3 FDA UDI

Identifiers

Catalog Number
WZ-1-1013 FDA UDI
Primary DI / UDI-DI
B046WZ110130 FDA UDI
510(k) Number
K012800 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Coated unicondylar knee tibia prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Coated unicondylar knee tibia prosthesis

Uni Tibial Tray by Signal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated unicondylar knee tibia 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 7744e966-3d1a-42cc-9ec3-8673d9b9c577 36 fields · synced Jun 8, 2026