Itotal Identity 3DP Porous Knee

iTotal Identity CR 3DP Porous Femur Hybrid iJigs Right

Registry build 21.09.26
2manufacturers in China registered for this device type
6catalogue numbers in this listing

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 iTotal Identity 3DP Porous Knee
Listed by restor3d, inc., United States
FDA product code OOG
Device type Knee Arthroplasty Implantation System
Device class Class 2
Regulation 21 CFR 888.3560
Establishment Complaint-file establishment, Manufacturer
510(k) K243768
Record published 2025-12-02

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries expiry date, serial number

Catalogue Numbers

Catalogue numbers for iTotal Identity 3DP Porous Knee
Catalogue number Size Status
TCR-000-SPEC-010121 In distribution
TCR-000-D005-010111 In distribution
TCR-000-D005-020111 In distribution
TCR-000-SPEC-010131 In distribution
TCR-000-SPEC-020131 In distribution
TCR-000-SPEC-020121 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

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