Large Cannulated Screws

Cannulated HIP PIN 120MM

Registry build 21.09.26
2manufacturers in China registered for this device type
22catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

All of them in Shanghai. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code JDO
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for Large Cannulated Screws
Listed by Smith & Nephew, Inc., United States
FDA product code JDO
Device type Device, Fixation, Proximal Femoral, Implant
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2017-11-13
Record revised 2025-08-08 (version 6)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Large Cannulated Screws
Catalogue number Size Status
121662 In distribution
121672 In distribution
121654 In distribution
121659 In distribution
121675 In distribution
121661 In distribution
121663 In distribution
121669 In distribution
121656 In distribution
121671 In distribution
121655 In distribution
121670 In distribution
121667 In distribution
121664 In distribution
121660 In distribution
121665 In distribution
121657 In distribution
121673 In distribution
121666 In distribution
121668 In distribution
121658 In distribution
121674 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
BMP Compression HIP Screw Biomet Orthopedics 112
DHS Synthes Gmbh 93
THP™ Hip Fracture Plating System Biomet Orthopedics 74
Percutaneous Compression Plate (Pc.c.p) Orthofix SRL 69
Proform Hip System Globus Medical, Inc. 51
Conquest FN Smith & Nephew, Inc. 31
CHS Smith & Nephew, Inc. 26
TSP HIP FX Plating SYSTEM4.5MM Cortical NON – Locking Screw Biomet Orthopedics 13
TSP HIP FX Plating SYSTEM4.5MM Cortical Locking Screw Biomet Orthopedics 12
TSP HIP FX Plating SYSTEM7.5MM Telescoping LAG Screw Biomet Orthopedics 6
Dhhs Synthes Gmbh 6
3P Hip System Orthopediatrics, Corp 5

Showing 12 of 112. All products under Device, Fixation, Proximal Femoral, Implant

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213126 2022-09-29
K193029 2020-02-28
K172785 2017-12-22
K152686 2016-03-17
K080434 2008-04-10

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