Aequalis Reversed II

Glenoid Sphere/Humeral Head Trial Handle

Registry build 21.09.26
53manufacturers in China registered for this device type
77catalogue 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 Aequalis Reversed II
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 2024-04-01 (version 4)

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
Sizes Outer diameter 6.5 to 42 mm; length 100 to 210 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Aequalis Reversed II
Catalogue number Size Status
MWB190 Thickness: +9mm In distribution
MWB087 Lateralized In distribution
MWG904 Centered In distribution
MWB195 Outer Diameter 42 mm In distribution
MWB186 Lateralized In distribution
MWB175 Outer Diameter 36 mm In distribution
MWG907 Centered In distribution
MWD180 Centered In distribution
MWD193 Centered In distribution
MWG909 Outer Diameter 39 mm In distribution
MWB185 Thickness: +6mm In distribution
MWB170 Length 100 mm In distribution
MWB972 Lateralized In distribution
MWB084 Thickness: +12mm In distribution
MWG902 Thickness: +6mm In distribution
MWB152 Length 180 mm In distribution
MWG903 Thickness: +8mm In distribution
MWD185 Outer Diameter 42 mm In distribution
MWF710 In distribution
MWB153 Length 210 mm In distribution
MWB181 Lateralized In distribution
MWB161 Length 150 mm In distribution
MWB192 Outer Diameter 36 mm In distribution
MWB090 Thickness: +12mm In distribution
MWD140 Color: GRAY In distribution
MWB088 Lateralized In distribution
MWB172 Outer Diameter 15 mm In distribution
MWB151 Outer Diameter 9 mm In distribution
MWG906 Outer Diameter 39 mm In distribution
MWB970 Thickness: +6mm In distribution
MWB163 Length 210 mm In distribution
MWD184 Thickness: +4mm In distribution
MWD139 Color: BLUE In distribution
MWF729 In distribution
MWD182 Outer Diameter 36 mm In distribution
MWB141 Outer Diameter 6.5 mm In distribution
MWB143 Outer Diameter 6.5 mm In distribution
MWB083 Thickness: +9mm In distribution
MWD044 In distribution
MWB176 Outer Diameter 42 mm In distribution
MWB260 In distribution
MWB142 Length 180 mm In distribution
MWB250 In distribution
MWB150 Outer Diameter 9 mm In distribution
MWD183 Centered In distribution
MWB180 Thickness: +6mm In distribution
MWD223 In distribution
MWB194 Outer Diameter 36 mm In distribution
MWG905 Lateralized In distribution
MWB081 Lateralized In distribution
MWD181 Thickness: +4mm In distribution
MWB191 Thickness: +9mm In distribution
MWB105 In distribution
MWB971 Lateralized In distribution
MWB080 Lateralized In distribution
MWB089 Lateralized In distribution
MWB085 Lateralized In distribution
MWB086 Lateralized In distribution
MWB082 Lateralized In distribution
MWD194 Thickness: +4mm In distribution
MWB160 Length 100 mm In distribution
MWD190 Centered In distribution
MWB187 Lateralized In distribution
MWD195 Outer Diameter 42 mm In distribution
MWD319 In distribution
MWD191 Thickness: +4mm In distribution
MWB171 Length 150 mm In distribution
MWG901 Thickness: +4mm In distribution
MWD192 Outer Diameter 36 mm In distribution
MWB140 Outer Diameter 6.5 mm In distribution
MWG908 Thickness: +4mm In distribution
MWB162 Outer Diameter 12 mm In distribution
MWB182 Thickness: +12mm In distribution
MWB193 Outer Diameter 42 mm In distribution
MWB981 Lateralized In distribution
MWB982 Lateralized In distribution
MWB980 Thickness: +6mm 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