# Spiritus Technologies, LLC

- Location (FDA's records): Lenexa, KS
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: BSK (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 0 (0 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
- Posey Co.: 1 (https://510kreport.com/company/posey)
- Mallinckroot, Inc.: 1 (https://510kreport.com/company/mallinckroot)
- Extracorporeal Medical Specialities, Inc.: 1 (https://510kreport.com/company/extracorporeal-medical-specialities)
- Mallinckrodt Critical Care: 1 (https://510kreport.com/company/mallinckrodt-critical-care)

## Recent decisions
- K112915: Spirtius Cuff Inflation Syringe (May 25, 2012)

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