Data / Medical devices / United States / Hollywog, LLC
Hollywog, LLC: FDA-registered device maker in Chattanooga, TN, United States, 2 510(k) clearances
Hollywog, LLC is registered with the FDA (registration 3008585473) in Chattanooga, TN, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 22, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008585473
- Address
- 100 Cherokee Boulevard, Chattanooga, TN, United States, 37405
- Owner or operator
- Hollywog, LLC (10038742)
- Roles
- Manufacturer
- First device listed
- October 5, 2015
- Registered through
- 2026
- Brand names listed
- Modpod, TensTouch, WiTouch Pro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Equipment, Traction, Powered | ITH | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Stimulator, Electrical, Transcutaneous, For Arthritis | NYN | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 22, 2017 | K171599 | WiTouch Pro, WiTouch, Neubac | NUH | Substantially Equivalent | Hollywog, LLC | accessdata.fda.gov |
| August 13, 2015 | K150695 | Modpod | ITH | Substantially Equivalent | Hollywog, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Equipment, Traction, Powered
- All makers of Stimulator, Electrical, Transcutaneous, For Arthritis
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Massager, Therapeutic, Electric
Updated September 22, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.