# Sensormed

- Location (FDA's records): Knoxville, TN
- FDA decisions: 2 (2010–2012): 2 510(k) clearances
- Product codes: FST (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (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
- Spinal Elements, Inc.: 1 (https://510kreport.com/company/spinal-elements)

## Its most-cited devices
- K101496: Cablecap Model: WLF, STZ, Acm (2010), cited by 1

## Recent decisions
- K113330: Cablecap (Jan 12, 2012)
- K101496: Cablecap Model: WLF, STZ, Acm (Sep 14, 2010)

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