DynaFORCE™

DynaFORCE MotoCLIP/HiMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis

Registry build 21.09.26
7manufacturers in China registered for this device type
24catalogue numbers in this listing
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Guangdong (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDR
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for DynaFORCE™
Listed by Crossroads Extremity Systems LLC, United States
FDA product code JDR
Device type Staple, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Complaint-file establishment, Manufacturer
510(k) K142727
Record published 2019-12-11
Record revised 2025-03-17 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Distribution end date 2024-08-22

Catalogue Numbers

Catalogue numbers for DynaFORCE™
Catalogue number Size Status
DynaFORCE 25mm Clip Prep Kit In distribution
7009-0909KT 9mm x 9mm x 9mm In distribution
DynaForce 12x12x12mm MotoClip Max C Sterile Kit 18mm x 14mm x 14mm In distribution
7118-2020KT 18mm x 20mm x 20mm In distribution
DynaFORCE 20mm Clip Prep Kit In distribution
DynaForce 9x9x9mm MotoClip Max C 18mm x 14mm x 14mm In distribution
7118-1414KT 18mm x 14mm x 14mm In distribution
7115-1818KT 15mm x 18mm x 18mm In distribution
7125-2222KT 25mm x 22mm x 22mm In distribution
DynaForce 10x10x10mm MotoClip Max C Implant Kit 18mm x 14mm x 14mm In distribution
DynaFORCE HiMax Implant Kit, 20 x 14 x 14 18mm x 22mm x 22mm In distribution
DynaFORCE 18mm Clip Prep Kit In distribution
7115-1515KT 15mm x 15mm x 15mm In distribution
7012-1212KT 12mm x 12mm x 12mm In distribution
DynaFORCE HiMax Implant Kit 18x18x14 18mm x 14mm x 14mm In distribution
7015-1515KT 15mm x 15mm x 15mm In distribution
7120-2020KT 20mm x 20mm x 20mm In distribution
7118-1818KT 18mm x 18mm x 18mm In distribution
DynaForce 15x15x15mm MotoClip Max C Sterile Kit 18mm x 14mm x 14mm In distribution
DynaFORCE 15mm Clip Prep Kit In distribution
DynaFORCE HiMax Implant Kit, 25 x 14 x 14 18mm x 22mm x 22mm In distribution
DynaForce, Standard Inserter, 15mm-S Withdrawn
DynaForce, Standard Inserter, 12mm Withdrawn
DynaForce, Standard Inserter, 9mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DynaBridge Fusion Orthopedics, LLC 156
Arthrex® Arthrex, Inc. 80
Staple, Fixation, Bone Smith & Nephew, Inc. 59
Compression Staple System Tornier Inc. 36
UNI-Clip Newdeal Sas 35
Z-Staple Z-Medical Gmbh & Co. KG 34
Orbitum Staple System CPM Medical Consultants, LLC. 32
OSStaple Biomedical Enterprises, Inc. 30
Acumed Acumed LLC 30
Stealthfix Intraosseous Fixation System Medartis Inc. 29
Staple, Fixation, Bone Stryker GmbH 29
Step Boss Biomedical Enterprises, Inc. 27

Showing 12 of 319. All products under Staple, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K181866 2018-08-09
K181410 2018-06-29

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of DynaFORCE™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Crossroads Extremity Systems LLC 510(k) number 2017-02-16 Class II Labeling mix-ups Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and labeled as 18mm x 14mm x 14mm. 20 units 2017-04-27

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