Dynatron® Ion™ Medium

2 catalogue numbers from ION-M, listed by Dynatronics Corp., United States, under Device, Iontophoresis, Other Uses. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (1), Guangdong (1).

Chinese manufacturers registered for FDA product code EGJ
Manufacturer City Province Registered as Device types
Top-rank Health Care Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
General Meditech, Inc. Shenzhen Guangdong Complaint-file establishment 3

Record

Regulatory record for Dynatron® ion™ Medium
Listed by Dynatronics Corp., United States
FDA product code EGJ
Device type Device, Iontophoresis, Other Uses
Device class Class 2
Regulation 21 CFR 890.5525
Record published 2015-11-20
Record revised 2023-10-26 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 41 to 80.6 °F
Sizes Area/surface area 1.3 to 1.8 Square inch
Distribution end date 2023-11-08

Catalogue Numbers

Catalogue numbers for Dynatron® ion™ Medium
Catalogue number Size Status
ION-M Area/Surface Area 1.8 Square inch Withdrawn
ION-M Area/Surface Area 1.3 Square inch Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Drionic TM General Meditech, Inc. 15
Chattanooga DJO, LLC 13
Richmar South Dakota Partners 12
BodyMed Iontophoresis Electrode Kit Drive DeVilbiss Healthcare 8
Trivarion Activatek, Inc. 4
Norco Activatek, Inc. 4
Performa Performance Health Supply, Inc. 4
BodyMed Boxout, LLC 4
IontoPatch LTS Therapy Systems, LLC 4
Dupel Blue Clearlake-Tech Inc 4
Ionto480 Buffered Iontophoresis Electrode Treatment Kit Axelgaard Manufacturing Co., Ltd. 4
ActivaTek Ionto4 Kit North Coast Medical, Inc. 3

Showing 12 of 68. All products under Device, Iontophoresis, Other Uses

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K060814 2006-06-14
K043047 2005-01-07

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