# Repro-Med Systems, Inc. Dba Rms Medical Products

- Location (FDA's records): New York, NY
- FDA decisions: 3 (2013–2019): 3 510(k) clearances
- Product codes: FPA (2), FRN (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Repro-Med Systems, Inc.: 2 (https://510kreport.com/company/repro-med-systems)
- Evans Medical, Inc.: 1 (https://510kreport.com/company/evans-medical)
- Marcal Medical, Inc.: 1 (https://510kreport.com/company/marcal-medical)

## Firms that cite its devices most
- Repro-Medical System, Inc., Dba Koru Medical Systems: 1 (https://510kreport.com/company/repro-medical-system-dba-koru-medical-systems)
- Repro-Med Systems, Inc. Dba Koru Medical Systems: 1 (https://510kreport.com/company/repro-med-systems-dba-koru-medical-systems)

## Its most-cited devices
- K162613: Integrated Catch-up Freedom Syringe Driver Infusion System (2017), cited by 2

## Recent decisions
- K180843: HIgH-Flo Super26 Subcutaneous Needle Sets (Apr 4, 2019)
- K162613: Integrated Catch-up Freedom Syringe Driver Infusion System (Aug 31, 2017)
- K122404: Model Number: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26 (May 6, 2013)

Source page: https://510kreport.com/company/repro-med-systems-dba-rms-medical-products