FDA.reportPublic FDA data

HOLLYWOG, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30085854733008585473HOLLYWOG, LLC1N2026-01-01100 Cherokee Boulevard Chattanooga TN US 37405

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00853096004014WiTouch - WiTouch brand over the counter transcutaneous electrical nerve simulator for analgesic pain relief in the lower back4233057778info@hollywog.com
00853096004021WiTouch Pro - WiTouch brand over the counter transcutaneous electrical nerve simulator to be used for temporary relief of pain associated with sore and aching muscles in the back due to strain from exercise or normal household and work activities and relief of pain of the upper and lower back associated with arthritis.4233057778info@hollywog.com
00853096004083Neubac - Neubac brand of over the counter transcutaneous electrical nerve stimulator for analgesic pain relief in the lower back.4233057778info@Hollywog.com
00853096004151Modpod - Modpod brand powered, static/intermittent, mobile traction system4233057778info@hollywog.com
10853096004158Modpod - Modpod brand powered, static/intermittent, mobile traction system4233057778info@hollywog.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1348671801667394K171599WiTouch Pro, WiTouch, NeubacNUH2017-09-22
1348671179600277K150695ModpodITH2015-08-13
1348671688807089

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NUH12017-09-22
ITH12015-08-13

PMN#

GUDID#