17 results · 30ms · Sources: EU EUDAMED, US FDA

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HOLLYWOG, LLC

FDA registration
HOLLYWOG, LLC·4 products·🇺🇸 United States

WiTouch Pro

FDA UDI
HOLLYWOG, LLC·00853096004021·WiTouch brand over the counter transcutaneous e...

WiTouch

FDA UDI
HOLLYWOG, LLC·00853096004014·WiTouch brand over the counter transcutaneous e...

Modpod

FDA UDI
HOLLYWOG, LLC·00853096004151·Modpod brand powered, static/intermittent, mobi...

Neubac

FDA UDI
HOLLYWOG, LLC·00853096004083·Neubac brand of over the counter transcutaneous...

WITOUCH

FDA Adverse Event
Malfunction ·HOLLYWOG, LLC·Product code NUH·October 13, 2016

MODPOD

FDA Adverse Event
Malfunction ·HOLLYWOG, LLC·Product code ITH·November 9, 2017

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 10, 2018

WITOUCH

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·August 8, 2016

WITOUCH

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 11, 2017

WITOUCH

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·April 5, 2016

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code GZJ·May 26, 2015

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 23, 2019

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 23, 2019

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 30, 2019

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 16, 2019

WITOUCH PRO

FDA Adverse Event
Injury ·HOLLYWOG, LLC·Product code NUH·July 16, 2019