# Neotonus, Inc.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 4 (1998–2001): 4 510(k) clearances
- Product codes: KPI (2), IPF (1), KOI (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 4 (0 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
- Hollister, Inc.: 2 (https://510kreport.com/company/hollister)
- Utah Medical Products, Inc.: 1 (https://510kreport.com/company/utah-medical-products)
- Empi: 1 (https://510kreport.com/company/empi)

## Firms that cite its devices most
- Fotona D.O.O.: 2 (https://510kreport.com/company/fotona-doo)
- BTL Industries, Inc.: 2 (https://510kreport.com/company/btl-industries)

## Its most-cited devices
- K973929: Neotonus MS-101 Magnetic Muscle Stimulator System (1998), cited by 2
- K973096: Neotonus Model 1000 Muscle Stimulator System (1998), cited by 2

## Recent decisions
- K002889: PNS Magnetic Stimulator System (Apr 6, 2001)
- K001903: Neocontrol Pelvic Floor Therapy System (Aug 29, 2000)
- K973096: Neotonus Model 1000 Muscle Stimulator System (Jun 12, 1998)
- K973929: Neotonus MS-101 Magnetic Muscle Stimulator System (May 21, 1998)

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