Who else makes this device?

Name: Push Patch Controlled Released 12.0
Brand: Push Patch Controlled Released 12.0

Physical Medicine › TherapeuticDevice, Iontophoresis, Other Uses

Push Patch Controlled Released 12.0

Push Patch Controlled Released 12.0 - Private labeled ActivaPatch IontoGo 12.0 iontophoresis wireless electrode

Registry build 21.09.26

2manufacturers in China registered for this device type

1catalogue number

1510(k) clearance

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 Push Patch Controlled Released 12.0
Listed by	North Coast Medical, Inc., United States
FDA product code	EGJ
Device type	Device, Iontophoresis, Other Uses
Device class	Class 2
Regulation	21 CFR 890.5525
Establishment	Repacker / relabeller, Manufacturer
Record published	2025-12-01

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, manufacturing date
Packaging	Master carton of 40

Catalogue Numbers

Catalogue numbers for Push Patch Controlled Released 12.0
Catalogue number	Size	Per pack	Status
4549		6	In distribution

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
K052019	2005-11-04

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.