Identity Imprint Knee Replacement System

PS Tibial Insert Trial Size 3 18MM Left AND Right

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance
3recalls on this code

Who Else Makes It

Concentrated in Shanghai (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OOG
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74

Record

Regulatory record for Identity Imprint Knee Replacement System
Listed by ConforMIS, Inc., United States
FDA product code OOG
Device type Knee Arthroplasty Implantation System
Device class Class 2
Regulation 21 CFR 888.3560
Establishment Remanufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K210191
Record published 2021-06-07
Record revised 2023-07-13 (version 3)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Identity Imprint Knee Replacement System
Catalogue number Size Status
TPS020164S01 In distribution
TPS020143S01 SIZE 3 14MM THICKNESS In distribution
TPS030183S01 SIZE 3 18MM THICKNESS In distribution
TPS301T02N01 tibial tray size 2 narrow In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy Microport Orthopedics Inc. 1,463
PointCloud Knee Instruments Unik Orthopedics, Inc 202
iTotal Identity CR ConforMIS, Inc. 138
My Knee Femoral Cutting Blocks Medacta International SA 60
iTotal® CR iPoly™ Insert Kit ConforMIS, Inc. 59
My Knee Tibial Cutting Blocks Medacta International SA 48
My Knee Femoral Cutting Blocks MIS Medacta International SA 42
My Knee Tibial Cutting Blocks MIS Medacta International SA 36
iTotal® Identity Cruciate Retaining Knee Replacement System ConforMIS, Inc. 27
iTotal® CR iPoly® XE Insert Kit ConforMIS, Inc. 16
Zimmer Patient Specific Instruments Materialise NV 12
iTotal Identity CR Knee Replacement System ConforMIS, Inc. 12

Showing 12 of 95. All products under Knee Arthroplasty Implantation System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K203421 2021-04-19

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Identity Imprint Knee Replacement System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
ConforMIS, Inc. 510(k) number 2024-03-11 Class II Process design Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot 540287. It was confirmed that Lot 540287 and Lot 508287 were swapped between the pouching and final pack. 3 units

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2015-08-31 Class II Process design May contain small amounts of ethylene glycol residue 7 units 2016-03-02
2015-08-31 Class II Process design May contain small amounts of ethylene glycol residue 71 units 2016-03-02
2015-08-31 Class II Process design May contain small amounts of ethylene glycol residue 6 units 2016-03-02

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer