510(k) Report

FDA applicant

Hollywog, LLC

Chattanooga, TN4 decisions2012–20170 recalls

FDA records 4 decisions for Hollywog, LLC (Chattanooga, TN) from 2012 to 2017: 4 510(k) clearances. Most are in product codes NUH (Stimulator, Nerve, Transcutaneous…) and ITH (Equipment, Traction, Powered). Its devices cite 8 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Hollywog, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2012: 22015: 12017: 1
2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Hollywog, LLC by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NUHStimulator, Nerve, Transcutaneous, Over-The-Counter2decisions
  • ITHEquipment, Traction, Powered1decision
  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

Whose devices does it build on?

Its devices cite 8 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 times; 1 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K120500The Pain Pilot (a.K.a Pain Pilot)Hollywog, LLC · 20122cite it
  • K120398Witouch ProHollywog, LLC · 20122cite it

What has FDA decided for it lately?

  • K171599WiTouch Pro, WiTouch, NeubacHollywog, LLC · 2017
  • K150695ModpodHollywog, LLC · 2015
  • K120500The Pain Pilot (a.K.a Pain Pilot)Hollywog, LLC · 2012
  • K120398Witouch ProHollywog, LLC · 2012

All 4 as Hollywog, LLC →