# Common Sense, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2007–2009): 2 510(k) clearances
- Product codes: CEN (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- Femtek,Llc.: 1 (https://510kreport.com/company/femtek)
- Pro-Lab, Inc.: 1 (https://510kreport.com/company/pro-lab)

## Firms that cite its devices most
- Clinical Innovations, Inc.: 1 (https://510kreport.com/company/clinical-innovations)

## Its most-cited devices
- K071100: Amniscreen Home Detection Liner Kit (2007), cited by 1

## Recent decisions
- K091287: VS-Sense Test (Aug 31, 2009)
- K071100: Amniscreen Home Detection Liner Kit (Oct 15, 2007)

Source page: https://510kreport.com/company/common-sense