# Medspira, LLC

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 3 (2012–2025): 3 510(k) clearances
- Product codes: KLA (2), FFX (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Clinical Innovations, Inc.: 1 (https://510kreport.com/company/clinical-innovations)
- Urodynamix Technologies, Ltd.: 1 (https://510kreport.com/company/urodynamix-technologies)
- Sierra Scientific Instruments, Inc.: 1 (https://510kreport.com/company/sierra-scientific-instruments)
- Mui Scientific: 1 (https://510kreport.com/company/mui-scientific)

## Firms that cite its devices most
- Thd Spa: 2 (https://510kreport.com/company/thd)

## Its most-cited devices
- K120088: Mcompass Anorectal Manometry System (2012), cited by 3
- K143031: mcompass Biofeedback Anorectal Manometry System (2015), cited by 1

## Recent decisions
- K252605: mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001) (Dec 5, 2025)
- K143031: mcompass Biofeedback Anorectal Manometry System (Jul 7, 2015)
- K120088: Mcompass Anorectal Manometry System (Mar 29, 2012)

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