U2 Total Knee System

Patellar drill guide, asymmetric onset, NON-CEM, XXL, 41mm

Registry build 21.09.26
53manufacturers in China registered for this device type
220catalogue numbers in this listing
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (24), Guangdong (7), Zhejiang (6). 29 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LXH
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Jinsheng Plastic Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17

Showing 12 of 53. All 53 manufacturers in China registered for Orthopedic Manual Surgical Instrument

Record

Regulatory record for U2 Total Knee System
Listed by United Orthopedic Corp., Taiwan
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Contract manufacturer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2024-11-22
Record revised 2020-04-06 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for U2 Total Knee System
Catalogue number Size Status
9403-2530 In distribution
9303-5130 In distribution
9304-3009 In distribution
9323-5337 In distribution
9404-2002-TE In distribution
9304-2440 In distribution
9304-2650 In distribution
9323-2716 In distribution
9423-1301 In distribution
9304-2665 In distribution
9303-2014-RA In distribution
9404-7301-RA 430mm In distribution
9303-2245-TF In distribution
9304-2435 In distribution
9404-2001-TD In distribution
9304-2455 In distribution
9303-2175-RA In distribution
9401-4205-TE In distribution
9403-2123-RE 3°, left In distribution
9403-2223-RE 3°, right In distribution
9303-2551 #5 In distribution
9304-2330-RA In distribution
9304-5107-TA In distribution
9303-2302-RA In distribution
9403-5002-RA In distribution
9323-5338 In distribution
9404-2430-RA In distribution
9303-5314-RB In distribution
9403-2125-RN In distribution
9401-5115-TB In distribution
9304-2511 In distribution
9304-3007 In distribution
9403-2220-RN In distribution
9403-2125-RF In distribution
9303-2250-TF In distribution
9304-5111 In distribution
9403-5003 In distribution
9404-2301-RB In distribution
9303-2255-TF In distribution
9303-2174-RA In distribution
9403-5002 In distribution
9304-3008 In distribution
9403-1202-RB In distribution
9303-2260-TF In distribution
9303-2225-TF In distribution
9423-2302 In distribution
9404-2460-RA In distribution
9404-2031 In distribution
9323-5335 In distribution
9403-2815 In distribution
9403-2310-RB In distribution
9304-2625 In distribution
9403-2120-RN In distribution
9303-2230-TF In distribution
9403-5318 In distribution
9403-2225-RN In distribution
9304-2470 In distribution
9403-5331-RB In distribution
9303-2155-RC In distribution
9304-2310 In distribution
9303-2220-TF In distribution
9403-2120-RF In distribution
9303-2240-TF In distribution
9303-2165-RC In distribution
9404-2032 In distribution
9403-5376 In distribution
9303-2014-RA In distribution
9401-5323-TB In distribution
9323-5312 In distribution
9404-2901-RA In distribution
9303-5312-RB In distribution
9323-2717 In distribution
9304-2330 In distribution
9304-3005-RT In distribution
9401-5116-TB In distribution
9401-5117-TB In distribution
9303-3207-RA In distribution
9303-2452-RD In distribution
9404-5104 In distribution
9303-2215-TF In distribution
9403-2520 In distribution
9304-2670 In distribution
9323-5339 In distribution
9304-2350-RA In distribution
9304-2425 In distribution
9304-2310-RA In distribution
9304-2370 In distribution
9304-2615 In distribution
9404-2901 In distribution
9303-5131 In distribution
9403-5111-RB In distribution
9403-2322-RC In distribution
9304-3009 In distribution
9303-2235-TF In distribution
9304-2410 In distribution
9303-5312-RB In distribution
9323-5132 In distribution
9403-2715 In distribution
9403-5309 In distribution
9303-2210-TF In distribution
9404-2001-TE In distribution
9304-2450 In distribution
9403-5308 In distribution
9304-3007 In distribution
9403-2140-RA In distribution
9401-5324-TB In distribution
9303-3207-RB In distribution
9304-2101-RB In distribution
9304-1103-RA In distribution
9304-2655 In distribution
9404-2903 In distribution
9304-2551 In distribution
9403-2223-RN In distribution
9303-2012-RA In distribution
9303-2171-RA In distribution
9303-2311-RA #1 In distribution
9304-2460 In distribution
9304-2640 In distribution
9323-2736 In distribution
9303-2173-RA In distribution
9404-2220-RA In distribution
9304-2630 In distribution
9403-1202-RB In distribution
9323-2733 In distribution
9404-2240-RA In distribution
9404-2002-TD In distribution
9403-5331 In distribution
9404-2902-RA In distribution
9404-2250-RA In distribution
9404-2903-RA In distribution
9303-2016-RA In distribution
9404-2612 In distribution
9404-2440-RA In distribution
9303-2303 In distribution
9304-2620 In distribution
9304-2465 In distribution
9303-5106 In distribution
9403-2321-RC In distribution
9403-2620 In distribution
9304-2445 In distribution
9403-7101-TE In distribution
9304-2561 In distribution
9404-1105 430mm In distribution
9401-5325-TB In distribution
9404-5307 430mm In distribution
9423-5316 In distribution
9304-2660 In distribution
9423-5317 In distribution
9323-5318 In distribution
9403-2240-RA In distribution
9403-2132 In distribution
9304-2320 In distribution
9304-2340 In distribution
9303-2172-RA In distribution
9403-2630 In distribution
9404-2002-TF In distribution
9323-2735 In distribution
9404-2001-TF In distribution
9304-2521 In distribution
9404-2902 In distribution
9323-2731 In distribution
9403-5310 In distribution
9404-2450-RA In distribution
9323-2711 In distribution
9323-2734 In distribution
9303-2105-TB In distribution
9304-2645 In distribution
9403-2123-RF In distribution
9403-5109 In distribution
9403-2000 In distribution
9304-2571 In distribution
9304-2610 In distribution
9304-2320-RA In distribution
9403-5307 In distribution
9404-2230-RA In distribution
9304-2430 In distribution
9304-7103 In distribution
9404-2420-RA In distribution
9323-5310 In distribution
9304-2340-RA In distribution
9303-5301-RE In distribution
9304-2350 In distribution
9401-5329-TB In distribution
9323-5334 In distribution
9323-5333 In distribution
9304-2370-RA In distribution
9303-2307 7°, right In distribution
9401-5312-TG In distribution
9404-5105 In distribution
9423-2005 In distribution
9404-2302-TD In distribution
9403-2220-RF In distribution
9303-5314-RB In distribution
9303-5117-TC In distribution
9404-2611 In distribution
9304-2415 In distribution
9323-5340 In distribution
9304-2635 In distribution
9304-2531 In distribution
9304-5104-RA In distribution
9404-1301 In distribution
9304-3008 In distribution
9423-5315 In distribution
9304-2360-RA In distribution
9403-2223-RF In distribution
9323-5336 In distribution
9323-2732 In distribution
9303-2016-RA In distribution
9403-5311 In distribution
9304-2201 In distribution
9304-2541 In distribution
9303-5311-TB In distribution
9304-2420 In distribution
9403-5377 In distribution
9403-2225-RF In distribution
9404-2260-RA In distribution
9303-2012-RA In distribution
9304-2000-RA In distribution
9403-2123-RN In distribution
9304-2360 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Razek Equipamentos Razek Equipamentos Ltda 11,578
Orthopedic Manual Surgical Instrument Globus Medical, Inc. 4,784
Instrument Howmedica Osteonics Corp 4,539
Orthopedic Manual Surgical Instrument Ortho Development Corp. 4,076
Knee Instruments Medacta International SA 3,944
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 3,420
Arthrex® Arthrex, Inc. 3,106
Spine Instruments Medacta International SA 2,892
Orthopedic Manual Surgical Instrument Medtronic Sofamor Danek, Inc. 2,766
Hip Instruments Medacta International SA 1,904
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 1,756
ReLine Nuvasive, Inc. 1,208

Showing 12 of 9,501. All products under Orthopedic Manual Surgical Instrument

Recalls Naming This Product

4 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of U2 Total Knee System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
United Orthopedic Corp. UDI-DI 2026-05-20 Class II Process design Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. 2
United Orthopedic Corp. UDI-DI 2026-05-20 Class II Process design Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail. 2
United Orthopedic Corp. UDI-DI 2026-03-19 Class II Device Design Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. 3
United Orthopedic Corp. UDI-DI 2026-03-19 Class II Device Design Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant. 3

Recalls

1 of these is 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
2017-02-10 Class II Device Design The locking lever pin component of the femoral driver may become deformed and break, resulting in malfunction during surgery and causing the device to become inoperable. 33 units 2017-06-28

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