# Regenesis Biomedical, Inc.

- Location (FDA's records): Scottsdale, AZ
- FDA decisions: 4 (1997–2023): 4 510(k) clearances
- Product codes: ILX (3), IMJ (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mrt, Inc.: 1 (https://510kreport.com/company/mrt)
- Viatherm Therapeutics, LLC: 1 (https://510kreport.com/company/viatherm-therapeutics)

## Its most-cited devices
- K091791: Provant System, Model 4201 (2010), cited by 1

## Recent decisions
- K223620: Reprieve by RegenesisTM (May 24, 2023)
- K131979: Provant Therapy System (Dec 13, 2013)
- K091791: Provant System, Model 4201 (Apr 7, 2010)
- K972093: Regenesis Model 42 (Oct 21, 1997)

Source page: https://510kreport.com/company/regenesis-biomedical