Complete Control System Gen2

The COMPLETE CONTROL System Gen2 is a controller for external powered upper limb prostheses. It acquires the user’s muscle signals noninvasively and uses pattern recognition to control…

Registry build 21.09.26

The COMPLETE CONTROL System Gen2 is a controller for external powered upper limb prostheses. It acquires the user’s muscle signals noninvasively and uses pattern recognition to control compatible prosthetic components.

The embedded system combines a main processor with device and electromyography interface cables and a calibration button. It is used alongside an upper limb prosthesis and draws power without requiring an additional battery.

Listed Item

The COMPLETE CONTROL System Gen2 is an advanced control solution designed to provide the functionality of a powered myoelectric prosthesis for upper extremity amputees. The COMPLETE CONTROL System Gen2 employs pattern recognition technology to non-invasively acquire user-specific muscle signals for the control of industry-standard upper extremity prostheses.

Fitting and Compatibility

The system includes the CONTROLROOM application and a communicator dongle to support configuration. It is validated for specified elbow, wrist and hand components listed in the user manual. Its use is limited to external prosthetic fittings of the upper limbs.

47manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Guangdong (29), Jiangsu (4), Zhejiang (4). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GXY
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Shenzhen Konmed Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
China Qingdao Bright Medical Manufacturing Co., Ltd. Qingdao Shandong Contract manufacturer 8
Pine Moon Electronics Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Top-rank Health Care Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
Omron (Dalian) Co., Ltd. (Plant 1) Dalian Liaoning Contract manufacturer 7
Shenzhen Zifound Infonet Technology Co., Ltd. Shenzhen, Guandong Guangdong Contract manufacturer 2
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Taizhou Chenguang Import AND Export Trading Co., Ltd. Taizhou Jiangsu Exporter 25

Showing 12 of 47. All 47 manufacturers in China registered for Electrode, Cutaneous

Record

Regulatory record for Complete Control System Gen2
Listed by Coapt LLC, United States
FDA product code GXY
Device type Electrode, Cutaneous
Device class Class 2
Regulation 21 CFR 882.1320
Establishment Remanufacturer, Complaint-file establishment, Manufacturer
510(k) K191083
Record published 2019-06-12
Record revised 2025-05-22 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Complete Control System Gen2
Catalogue number Size Status
1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rhythmlink® Rhythmlink International, LLC 455
waveguard Eemagine Medical Imaging Solutions Gmbh 166
Espire Elbow Hybrid College Park Industries 138
Technomed Europe Technomed Engineering B.V. 126
Cadwell Technomed Engineering B.V. 111
The Electrode Store Impulse Technology LLC 109
Electrode, Cutaneous Gmdasz Manufacturing Co., Ltd. 99
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 93
AdvanTrode Pepin Manufacturing, Inc. 78
Uni-Patch Cardinal Health 77
Alpha WillowWood Global LLC 68
Espire Elbow Pro College Park Industries 67

Showing 12 of 1,006. All products under Electrode, Cutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223738 2023-01-11
K223605 2022-12-30
K191083 2019-05-24
K190416 2019-04-04
K162891 2017-04-14

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2023-10-02 Class II Process design Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged. 247 devices
2023-10-02 Class II Process design Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged. 109 devices

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