DynaForce MotoBAND Max

The DynaForce™ MotoBAND™ Max Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of…

Registry build 21.09.26

The DynaForce™ MotoBAND™ Max Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. Certain plates in the system are compatible with the MotoCLIP/DynaForce Superelastic Fixation System.

22manufacturers in China registered for this device type
30catalogue numbers in this listing
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
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 Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
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
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for DynaForce MotoBAND Max
Listed by Crossroads Extremity Systems LLC, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Complaint-file establishment, Manufacturer
510(k) K152306
Record published 2017-04-10
Record revised 2026-01-16 (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
Label carries lot or batch number
Distribution end date 2026-01-15

Catalogue Numbers

Catalogue numbers for DynaForce MotoBAND Max
Catalogue number Size Status
7100-ZA15 In distribution
7100-RP18 In distribution
7100-RD15 In distribution
7100-RD18 In distribution
7100-5H18 In distribution
7100-ZA18 In distribution
7100-ZB18 In distribution
7100-RP15 In distribution
7100-99PN In distribution
7100-5H15 In distribution
7100-99PN In distribution
7100-ZB15 In distribution
7100-TJ15 In distribution
7100-4H15 In distribution
7100-4H18 In distribution
7100-TJ18 In distribution
7100-ZA18 Withdrawn
7100-ZA15 Withdrawn
7100-5H18 Withdrawn
7100-RD18 Withdrawn
7100-ZB15 Withdrawn
7100-RP18 Withdrawn
7100-TJ18 Withdrawn
7100-ZB18 Withdrawn
7100-5H15 Withdrawn
7100-4H18 Withdrawn
7100-4H15 Withdrawn
7100-RD15 Withdrawn
7100-RP15 Withdrawn
7100-TJ15 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253178 2026-01-06
K230591 2023-09-29
K223342 2023-03-30
K190658 2019-04-12
K181872 2019-02-19
K160300 2016-04-22
K152306 2015-12-11

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