# Rehabilicare, Inc.

- Location (FDA's records): New Brighton, MN
- FDA decisions: 4 (1997–2002): 4 510(k) clearances
- Product codes: GZJ (3), IPF (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 9 (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
- Medical Devices, Inc.: 3 (https://510kreport.com/company/medical-devices)
- Mentor Corp.: 1 (https://510kreport.com/company/mentor)
- Staodyne, Inc.: 1 (https://510kreport.com/company/staodyne)

## Firms that cite its devices most
- Cefar Medical AB: 2 (https://510kreport.com/company/cefar-medical)
- Vertis Neuroscience, Inc.: 2 (https://510kreport.com/company/vertis-neuroscience)
- Care Rehab, Inc.: 1 (https://510kreport.com/company/care-rehab)
- Care Rehab and Orthopaedic: 1 (https://510kreport.com/company/care-rehab-and-orthopaedic)
- Bioinduction Limited: 1 (https://510kreport.com/company/bioinduction)
- Lorenz Biotech S.P.A.: 1 (https://510kreport.com/company/lorenz-biotech)

## Its most-cited devices
- K982410: SMP-Plus,SX-Plus,SX Model # 49XX Series 9 Volt Tens Device (1998), cited by 4
- K971542: Ortho DX Neuromuscular Stimulator (1997), cited by 3
- K022405: Modification to Promax-XP, Tens and Microcurrent Device; Promax-Tens, Tens Device; Promax-Libra, Tens Device; Promax-Mic (2002), cited by 2

## Recent decisions
- K022405: Modification to Promax-XP, Tens and Microcurrent Device; Promax-Tens, Tens Device; Promax-Libra, Tens Device; Promax-Mic (Aug 12, 2002)
- K011017: Promax-XP, Tens and Microcurrent Device; Promax-Tens, Tens Device; Promax-Libra, Tens Device; Promax-MC, Microcurrent (Sep 24, 2001)
- K982410: SMP-Plus,SX-Plus,SX Model # 49XX Series 9 Volt Tens Device (Nov 6, 1998)
- K971542: Ortho DX Neuromuscular Stimulator (Aug 14, 1997)

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