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Identity Imprint Porous CR

FDA UDI

Class II (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
Identity Imprint Porous CR FDA UDI
Generic Name
Cruciate-retaining total knee prosthesis FDA UDI
Device Name
IDENTITY IMPRINT POROUS CR TIBIAL TRAY SIZE 2 FDA UDI
Model / Reference
TCR-302-T02S-01 FDA UDI
Description
IDENTITY IMPRINT POROUS CR TIBIAL TRAY SIZE 2 FDA UDI

Identifiers

Catalog Number
TCR-302-T02S FDA UDI
Primary DI / UDI-DI
M572TCR302T02S011 FDA UDI
510(k) Number
K223316 FDA UDI
FDA Product Code
MBH FDA UDI
JWH FDA UDI
OOG FDA UDI
OIY FDA UDI
GMDN Term
Cruciate-retaining total knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
888.3560 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
MRI Safety
MR Conditional FDA UDI

Category: Cruciate-retaining total knee prosthesis

Identity Imprint Porous CR by Conformis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cruciate-retaining total knee prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI 698cf556-aa9e-4092-8f6e-cdde71efbda9 37 fields · synced May 30, 2026