HOLLYWOG, LLC

FDA Device Registration & Listing · Chattanooga, TN, US · Registration 3008585473

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008585473
FEI Number
3008585473
Entity Name
HOLLYWOG, LLC
City/State/Country
Chattanooga, TN, US
Establishment Address
100 Cherokee Boulevard, Chattanooga, TN 37405, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hollywog, LLC (Owner Number: 10038742)
Owner / Operator Contact Address
4860 Hixson Pike, Suite 168, Hixson, TN 37343, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K150695
PMA Number
N/A

All Registered Proprietary Names

TensTouch WiTouch Pro Modpod

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2022-05-03
NYN Stimulator, Electrical, Transcutaneous, For Arthritis Neurology Class 2 882.5890 2017-12-08
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2017-12-08
ITH Equipment, Traction, Powered Physical Medicine Class 2 890.5900 2015-10-05

Official Correspondent

Kaci Dupree

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hollywog, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3016460723 ZHEJIANG AOLIN INDUSTRY & TRADE CO., LTD. Lishui Zhejiang, CN
3032903908 TECHDERM LLC Palm Beach Gardens, FL, US
3030407739 CL MEDIX INC Chantilly, VA, US
3009079475 Aerotel Ltd. Holon Central, IL
3025350087 LENYO WORLD LTD Budapest, HU
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008585473. Last updated year: 2026. Please use registration number 3008585473 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.