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KineMatch® PFR System

FDA UDI

Class II (US FDA UDI)

by Kinamed, Inc.

Identity

Trade Name
KineMatch® PFR System FDA UDI
Generic Name
Patellofemoral joint prosthesis FDA UDI
Device Name
Custom PFR Primary Left FDA UDI
Model / Reference
Custom 100 FDA UDI
Description
Custom PFR Primary Left FDA UDI

Identifiers

Catalog Number
Custom 100 FDA UDI
Primary DI / UDI-DI
00818720011240 FDA UDI
FDA Product Code
KRR FDA UDI
GMDN Term
Patellofemoral joint prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3540 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

No

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

No

FDA UDI

Category: Patellofemoral joint prosthesis

KineMatch® PFR System by Kinamed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patellofemoral joint prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kinamed, Inc.

Sources (1)

  • FDA UDI 4b6f8bb7-787c-4238-baf4-f4c696d8c98a 34 fields · synced May 30, 2026