MyoCycle

FES cycle ergometer

Registry build 21.09.26
8manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Guangdong (6), Jiangsu (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GZI
Manufacturer City Province Registered as Device types
JKH Health Co., Ltd. Dongguan Guangdong Contract manufacturer 22
Suzhou Fast ATM Electric Co., Ltd. Suzhou Jiangsu Contract manufacturer 2
Shenzhen Dongdixin Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 18
Netop Industrial Company Limited Dongguan Guangdong Manufacturer 14
Devon Medical Products (Jiangsu) Ltd Nantong Jiangsu Repacker / relabeller 12
Guangzhou Longest Medical Technology Co., Ltd. Guangzhou Guangdong Manufacturer 9
Shenzhen XFT Medical Limited Shenzhen Guangdong Manufacturer 8
Xemis Medical Technology (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 6

Record

Regulatory record for MyoCycle
Listed by Myolyn, Inc, United States
FDA product code GZI
Device type Stimulator, Neuromuscular, External Functional
Device class Class 2
Regulation 21 CFR 882.5810
Establishment Manufacturer
Record published 2023-09-11

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 MyoCycle
Catalogue number Size Status
MC-2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
L300 Go System Bioness Medical, Inc. 22
RT300 Restorative Therapies Inc. 20
H200 Wireless System Bioness Medical, Inc. 20
Chattanooga DJO, LLC 17
Cionic Cionic 6
L100 Go System Bioness Medical, Inc. 4
MyndStep Myndtec Inc 4
ReGrasp Rehabtronics, Inc. 4
XFT Shenzhen XFT Medical Limited 3
RT200 Restorative Therapies Inc. 2
RehaStim 2 Hasomed Gmbh 2
H200 Wireless Bioness Medical, Inc. 2

Showing 12 of 53. All products under Stimulator, Neuromuscular, External Functional

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213925 2022-04-25
K170132 2017-04-25

Recalls

1 of these is 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 Closed
2022-07-19 Class II Device Design Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock. 45 devices 2024-09-23

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