# Medical Devices, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 49 (1977–2001): 49 510(k) clearances
- Product codes: GZJ (16), GXY (7), KNX (4), IPF (4), GEI (3), CAW (2), KOD (2), LIH (1), FWF (1), EYN (1), HRX (1), MKJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 6 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Rehabilicare, Inc.: 3 (https://510kreport.com/company/rehabilicare)
- Care Rehab, Inc.: 2 (https://510kreport.com/company/care-rehab)
- Healthonics, Inc.: 2 (https://510kreport.com/company/healthonics)
- Newlife Sciences, LLC: 1 (https://510kreport.com/company/newlife-sciences)
- Padpro, LLC: 1 (https://510kreport.com/company/padpro)
- Compex Technologies, Inc.: 1 (https://510kreport.com/company/compex-technologies)
- Mediphysics Pain Centers of America: 1 (https://510kreport.com/company/mediphysics-pain-centers-of-america)

## Its most-cited devices
- K895473: DSX (TM), Digital SX, Quantum DSX, Model 4700S (1989), cited by 4
- K935132: Home Microcurrent HMC (1994), cited by 2
- K923914: IF-II (TM), Model 7200 (1992), cited by 2
- K002280: Pad Pro Pediatric Electrode, Model Pad Pro 2602 (2001), cited by 1
- K872657: Ultrapac II SX Plus (TM) (1987), cited by 1
- K881082: GV 11 (TM), Model 9700 (1988), cited by 1

## Recent decisions
- K002280: Pad Pro Pediatric Electrode, Model Pad Pro 2602 (Feb 5, 2001)
- K930084: Micro-Arthroscope (Sep 1, 1995)
- K940012: Smartbrace Electrode (Dec 5, 1994)
- K943126: Electroflex (Dec 5, 1994)
- K935132: Home Microcurrent HMC (Mar 14, 1994)
- K934619: Flexmate (Feb 23, 1994)
- K924897: Xenon Endoscopic Illuminator, Model Xei-300 (Jul 6, 1993)
- K930053: Video Camera W/ Electronic Shutter Model Vce-10 (May 17, 1993)

Source page: https://510kreport.com/company/medical-devices