# Bionicare Medical Technologies, Inc.

- Location (FDA's records): Sparks, MD
- FDA decisions: 2 (2003–2005): 2 510(k) clearances
- Product codes: NYN (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 7 (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
- Murray Electronics: 1 (https://510kreport.com/company/murray-electronics)

## Firms that cite its devices most
- Pain Management Technologies: 2 (https://510kreport.com/company/pain-management-technologies)
- Vision Quest Industries, Inc.: 2 (https://510kreport.com/company/vision-quest-industries)
- Healthonics, Inc.: 1 (https://510kreport.com/company/healthonics)
- Rs Medical: 1 (https://510kreport.com/company/rs-medical)

## Its most-cited devices
- K030332: Modification to Bionicare Stimulator System, Model Bio-1000 (2003), cited by 5
- K052625: Bionicare Stimulator System, Model Bio-1000 (2005), cited by 2

## Recent decisions
- K052625: Bionicare Stimulator System, Model Bio-1000 (Dec 5, 2005)
- K030332: Modification to Bionicare Stimulator System, Model Bio-1000 (Jun 6, 2003)

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