Hollywog L L C

FDA Filings

This page includes the latest FDA filings for Hollywog L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008585473
FEI Number3008585473
NameHOLLYWOG, LLC
Owner & OperatorHollywog, LLC
Contact Address100 Cherokee Boulevard Suite 123
Chattanooga TN 37405 US
Official Correspondent
  • Chuck Thomas
  • x-423-3057777-101
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address100 Cherokee Boulevard Suite 123
Chattanooga, TN 37405 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
HOLLYWOG, LLC
Modpod 12.10002019-10-31
HOLLYWOG, LLC
Neubac 11.30002019-10-31
HOLLYWOG, LLC
WiTouch 11.15102019-10-31
HOLLYWOG, LLC
WiTouch Pro 11.15002019-10-23
HOLLYWOG, LLC
WiTouch Pro2017-12-08
HOLLYWOG, LLC
WiTouch Pro2017-12-08
Hollywog LLC
WiTouch Pro, WiTouch, Neubac2017-09-22
HOLLYWOG, LLC
Modpod2015-08-13
HOLLYWOG, LLC
THE PAIN PILOT (A.K.A PAIN PILOT)2012-08-20
HOLLYWOG, LLC
WITOUCH PRO2012-08-16

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