Conformity Stem

Dual offset broach handle, right

Registry build 21.09.26
53manufacturers in China registered for this device type
34catalogue 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 Conformity Stem
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 2022-06-28
Record revised 2023-05-03 (version 2)

Specifications

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

Catalogue Numbers

Catalogue numbers for Conformity Stem
Catalogue number Size Status
9110-1301-RB In distribution
9110-1302 In distribution
9110-7018 In distribution
9110-1301 In distribution
9110-1501-RB In distribution
9110-1501 In distribution
9110-1900 In distribution
9110-1502-RB In distribution
9110-1101-RB In distribution
9110-7016 In distribution
9110-1301-RA In distribution
9110-1102 In distribution
9110-1501-TB In distribution
9110-1301-RT In distribution
9110-1512 In distribution
9110-1101 In distribution
9110-7014 In distribution
9110-1502 In distribution
9110-4001 In distribution
9110-1301-TB In distribution
9110-1101-RA In distribution
9110-4101 In distribution
9110-7012 In distribution
9110-1501-RA In distribution
9110-2001 In distribution
9110-6101 In distribution
9110-1502-RA In distribution
9110-7010 In distribution
9110-6000-RA In distribution
9110-7008 In distribution
9110-6000-RB In distribution
9110-6000 In distribution
9110-6098 In distribution
9110-1511 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

4 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
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
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
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
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