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
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.
| 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
| 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
| 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 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
| 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
| 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.
| 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.