HI-DOW INTERNATIONAL INC.

FDA Registration(s)#

Registration, FEI, Name table
Registration	FEI	Name	Status	Initial importer	Expiration year	Address
3003895865	3003895865	HI-DOW INTERNATIONAL INC.	1	Y	2026-01-01	2555 Metro Blvd Maryland Heights MO US 63043

Registration key, Listing key, Premarket submission table
Registration key	Listing key	Premarket submission	Device	Product code	Decision date
21164	1591159904	K233461	Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A)	NUH	2024-01-19
21164	1835505649	K190617	Wrap accessory electrodes	GXY	2019-07-02
21164	2024112442	K181234	Self-adhesive Electrode	GXY	2018-08-07
21164	2045376036	K163393	Hi-Dow Wireless TENS/EMS System (Model HD-5N)	NUH	2017-08-04
21164	1944976521	K162663	WELL LIFE Rx Wireless TENS/EMS Stimulator, model WR-2603/2603A, WR-2604/2604A and WR-2605/2605A	GZJ	2017-01-17
21164	1533108119	K151693	Dr-Ho's Foot Pad Electrode	GXY	2015-10-09
21164	2045865931	K141076	GARMENT ELECTRODES	GXY	2014-11-14
21164	1611104686	K102598	HI-DOW-XP	NUH	2011-05-13
21164	1714290870	K072168	OTC ABDOMEN & THIGH SYSTEM, MODEL: WL-2410, WL-2411 AND WL-2412	NGX	2007-12-19
21164	1684168708	K071910	NITRILE POWDER FREE EXAMINATION GLOVES (BLUE), NITRILE POWDER FREE EXAMINATION GLOVES (PINK)	LZA	2007-09-06
21164	1927358015	K063660	OTC TENS FOR LOW BACK PAIN RELIEF, MODEL WL-2407	NUH	2007-02-07
21164	1053036589
21164	1054806754
21164	1122286134
21164	1344883264
21164	1531976434
21164	1580905652
21164	1814548085
21164	1821803810
21164	2018776282

Product code, Registration listing records, Latest decision table
Product code	Registration listing records	Latest decision
NUH	5	2024-01-19
GXY	4	2019-07-02
GZJ	1	2017-01-17
NGX	1	2007-12-19
LZA	1	2007-09-06