Orthopedic Manual Surgical Instrument

Glenoid Sphere/Anatomic Head Impactor Tip

Registry build 21.09.26
53manufacturers in China registered for this device type
34catalogue numbers in this listing
3recalls 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 Orthopedic Manual Surgical Instrument
Listed by Tornier Inc., United States
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2022-08-08
Record revised 2023-05-03 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, manufacturing date
Sizes Outer diameter 1.4 to 37 mm; length 90 mm; height 13.5 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Orthopedic Manual Surgical Instrument
Catalogue number Size Status
MWE123 In distribution
MWD222 Hex 3.5mm In distribution
MWA271 In distribution
ARS744000 In distribution
MWD221 Size: SHORT In distribution
9763611 In distribution
ARS778700 In distribution
MWE125 In distribution
HCS-040-14-D Outer Diameter 1.4 mm In distribution
9763601 Length 90 mm In distribution
MWA275 In distribution
ARS743500 In distribution
9763602 Length 90 mm In distribution
MWB337 SZH In distribution
MWA274 In distribution
9763604 Outer Diameter 15 mm In distribution
MWD425 In distribution
9763613 In distribution
9763605 Outer Diameter 17 mm In distribution
ARS779500 In distribution
MDI341 In distribution
ARS779400 In distribution
MWE124 In distribution
MWD423 In distribution
MWD218 Size: LONG In distribution
ARS744700 In distribution
MWF530 In distribution
ARS743000 In distribution
MWD424 In distribution
MWB236 In distribution
MWA210 In distribution
9763603 Outer Diameter 13 mm In distribution
MBO101 In distribution
MWA237 Height 13.5 mm 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

2 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
2022-05-03 Class II Device Design The device is unable to meet sterilization requirements when sterilized per instructions in an Aesculap container. 1066 units
2014-09-19 Class II Device Design Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer 38 2016-10-31
2009-10-16 Not classified Other The adapters are able to come apart when a retaining ring in the proximal end of the adapter can dislodge from the retaining ring groove and the two ends of the adapter fall apart and are unable to be reassembled without special tools and k 127 pieces 2012-04-11

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