Pediatric Extremity Combo K-Wire System

2 catalogue numbers from KIT-KWI-EXLAR, listed by Wishbone Medical Inc., United States, under Pin, Fixation, Smooth. 12 manufacturers in China are registered for this product code.

Registry build 21.09.26
12manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HTY
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Aplus (Guangzhou) Medical Technology Company Guangzhou Guangdong Contract manufacturer 6
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for Pediatric Extremity Combo K-Wire System
Listed by Wishbone Medical Inc., United States
FDA product code HTY
Device type Pin, Fixation, Smooth
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K173013
Record published 2019-03-19
Record revised 2025-12-01 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
Distribution end date 2020-09-16

Catalogue Numbers

Catalogue numbers for Pediatric Extremity Combo K-Wire System
Catalogue number Size Status
KIT-KWI-EXLAR Withdrawn
KIT-KWI-EXMED Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rondo’ Citieffe SRL 265
HNM Medical HNM Stainless, LLC. 232
Kmedic Teleflex Medical LLC 227
gSource Gsource, LLC. 221
MicroAire® Microaire Surgical Instruments LLC 213
Orthomed Ortho-MED, Inc. 163
mahe medical GmbH Mahe Intl., Inc. 160
Pin, Fixation, Smooth Key Surgical, LLC 134
Pin, Fixation, Smooth Stryker GmbH 134
Aptus Medartis Inc. 134
Key Surgical K-Wires and Steinmann Pins Key Surgical, LLC 126
PedFlex Flexible Nailing System Orthopediatrics, Corp 119

Showing 12 of 682. All products under Pin, Fixation, Smooth

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173013 2017-12-14

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