Hinge Pediatric Plating System

HINGE PLATE GUIDE WIRE Ø1.1mm -GEN2 - PACK OF 2

Registry build 21.09.26
53manufacturers in China registered for this device type
17catalogue 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 Hinge Pediatric Plating System
Listed by Orthopediatrics Canada ULC, Canada
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Manufacturer
Premarket notification Exempt
Record published 2024-04-11
Record revised 2025-05-13 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number
Storage Special storage condition: keep at room temperature
Sizes Outer diameter 1.1 mm; lumen/inner diameter 1.2 to 3.2 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Hinge Pediatric Plating System
Catalogue number Size Per pack Status
HP-AOH290 In distribution
HP-CSE200 In distribution
HP-CHL280 In distribution
HP-GWR250-PKG6 Outer Diameter 1.1 mm 6 In distribution
HP-GWR250 Outer Diameter 1.1 mm In distribution
HPDG110 Lumen/Inner Diameter 1.2 mm In distribution
HP-DGS210 In distribution
HPW150-PKG6 Outer Diameter 1.1 mm 6 In distribution
HP-CYE100 In distribution
HP-CYE200 In distribution
HPH100 In distribution
HP-SOS270 In distribution
HP-CSIN240 In distribution
HPW150-PKG2 Outer Diameter 1.1 mm 2 In distribution
HPC200 In distribution
HP-GWR250-PKG2 Outer Diameter 1.1 mm 2 In distribution
HPW150 Outer Diameter 1.1 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. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2024-07-04 Class II Process control During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX. 6 units
2020-04-03 Class III Nonconforming Material/Component The lot number on the pediatric orthopedic implant driver instrument handle does not match the lot number on the label. 3 units 2020-11-20
2019-10-02 Class II Device Design There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out. 31 devices 2020-10-26

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