# Hollywog, LLC

- Location (FDA's records): Chattanooga, TN
- FDA decisions: 4 (2012–2017): 4 510(k) clearances
- Product codes: NUH (2), ITH (1), GZJ (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Chattanooga Group, Inc.: 2 (https://510kreport.com/company/chattanooga-group)
- Omron Healthcare, Inc.: 1 (https://510kreport.com/company/omron-healthcare)
- Newmark, Inc.: 1 (https://510kreport.com/company/newmark)
- Endurance Therapeutics: 1 (https://510kreport.com/company/endurance-therapeutics)
- Empi: 1 (https://510kreport.com/company/empi)
- Compex Technologies, Inc.: 1 (https://510kreport.com/company/compex-technologies)

## Firms that cite its devices most
- Bayer Healthcare, LLC: 1 (https://510kreport.com/company/bayer-healthcare)
- Prizm Medical, Inc.: 1 (https://510kreport.com/company/prizm-medical)
- Easy Med Instrument Co., Ltd.: 1 (https://510kreport.com/company/easy-med-instrument)

## Its most-cited devices
- K120500: The Pain Pilot (a.K.a Pain Pilot) (2012), cited by 2
- K120398: Witouch Pro (2012), cited by 2

## Recent decisions
- K171599: WiTouch Pro, WiTouch, Neubac (Sep 22, 2017)
- K150695: Modpod (Aug 13, 2015)
- K120500: The Pain Pilot (a.K.a Pain Pilot) (Aug 20, 2012)
- K120398: Witouch Pro (Aug 16, 2012)

Source page: https://510kreport.com/company/hollywog