# Pain Relief Technologies

- Location (FDA's records): Beaverton, OR
- FDA decisions: 3 (2006–2012): 3 510(k) clearances
- Product codes: GZJ (1), NUH (1), NFO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K113724: Electropulse-Cosmetic (Feb 15, 2012)
- K062532: Electropulse - Low Back Pain (Feb 9, 2007)
- K051128: Electropulse (Mar 10, 2006)

Source page: https://510kreport.com/company/pain-relief-technologies