Itotal Identity CR

Itotal Identity CR Tibial Insert, NO Trial, Ipoly XE, Medial, 11MM, Left & Right

Registry build 21.09.26
2manufacturers in China registered for this device type
138catalogue 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 iTotal Identity CR
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
Record published 2019-09-30
Record revised 2022-03-23 (version 2)

Specifications

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

Catalogue Numbers

Catalogue numbers for iTotal Identity CR
Catalogue number Size Status
RCR010080C01 In distribution
RCR020100004 In distribution
RCR010000J14 In distribution
RCR020000F14 In distribution
RCR020140004 In distribution
RCR010200R11 In distribution
RCR020180N01 In distribution
RCR010000K14 In distribution
RCR020110004 In distribution
RCR020170004 In distribution
RCR020000E14 In distribution
RCR010000K04 In distribution
RCR020110014 In distribution
RCR020140J11 In distribution
RCR020200014 In distribution
RCR020160004 In distribution
RCR020080C11 In distribution
RCR020000K04 In distribution
RCR020000C14 In distribution
RCR020160014 In distribution
RCR010000R14 In distribution
RCR010000M14 In distribution
RCR020140014 In distribution
RCR010060A11 In distribution
RCR010000R04 In distribution
RCR010200004 In distribution
RCR020090014 In distribution
RCR020100014 In distribution
RCR010180014 In distribution
RCR020120004 In distribution
RCR010000P04 In distribution
RCR010060004 In distribution
RCR020200R01 In distribution
RCR020200R11 In distribution
RCR020000E04 In distribution
RCR020070B11 In distribution
RCR020150004 In distribution
RCR020130H01 In distribution
RCR020090D01 In distribution
RCR010070004 In distribution
RCR010190P11 In distribution
RCR020070B01 In distribution
RCR020000G04 In distribution
RCR020170014 In distribution
RCR020190P01 In distribution
RCR010100014 In distribution
RCR020060A11 In distribution
RCR020000N14 In distribution
RCR020000P14 In distribution
RCR020000P04 In distribution
RCR020100E11 In distribution
RCR020180N11 In distribution
RCR020000R04 In distribution
RCR010000G14 In distribution
RCR010080C11 In distribution
RCR020080004 In distribution
RCR020180004 In distribution
RCR010000L04 In distribution
RCR010180N11 In distribution
RCR010080014 In distribution
RCR020000N04 In distribution
RCR010090014 In distribution
RCR020150K01 In distribution
RCR010070B11 In distribution
RCR010000M04 In distribution
RCR010110F01 In distribution
RCR020090004 In distribution
RCR010090D11 In distribution
RCR010200014 In distribution
RCR010060014 In distribution
RCR010190004 In distribution
RCR020000J14 In distribution
RCR010000N04 In distribution
RCR020000H14 In distribution
RCR010070014 In distribution
RCR020000D04 In distribution
RCR020190004 In distribution
RCR020000L14 In distribution
RCR020060014 In distribution
RCR020110F11 In distribution
RCR010200R01 In distribution
RCR020120G01 In distribution
RCR010060A01 In distribution
RCR010000L14 In distribution
RCR020070004 In distribution
RCR020000A14 In distribution
RCR020100E01 In distribution
RCR010100004 In distribution
RCR010110004 In distribution
RCR020000D14 In distribution
RCR020060004 In distribution
RCR020080014 In distribution
RCR020000C04 In distribution
RCR020120014 In distribution
RCR010100E11 In distribution
RCR020000F04 In distribution
RCR020170M11 In distribution
RCR020130004 In distribution
RCR010110014 In distribution
RCR010190P01 In distribution
RCR020000R14 In distribution
RCR020000H04 In distribution
RCR010090D01 In distribution
RCR020170M01 In distribution
RCR020000B04 In distribution
RCR010080004 In distribution
RCR010190014 In distribution
RCR010100E01 In distribution
RCR020180014 In distribution
RCR010000P14 In distribution
RCR020160L11 In distribution
RCR020140J01 In distribution
RCR020000M04 In distribution
RCR010000J04 In distribution
RCR020200004 In distribution
RCR020090D11 In distribution
RCR020110F01 In distribution
RCR020000G14 In distribution
RCR020130014 In distribution
RCR020000K14 In distribution
RCR020000L04 In distribution
RCR010070B01 In distribution
RCR020000B14 In distribution
RCR020190014 In distribution
RCR020190P11 In distribution
RCR020150014 In distribution
RCR020000A04 In distribution
RCR020000M14 In distribution
RCR020060A01 In distribution
RCR010180N01 In distribution
RCR020150K11 In distribution
RCR020000J04 In distribution
RCR020130H11 In distribution
RCR020070014 In distribution
RCR301111301 In distribution
RCR020120G11 In distribution
RCR010110F11 In distribution
RCR020080C01 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
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
iTotal® PS iPoly® XE Insert Kit ConforMIS, Inc. 11

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

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