# Single Pass, Inc.

- Location (FDA's records): Lake Forest, CA
- FDA decisions: 2 (2024–2026): 2 510(k) clearances
- Product codes: GEI (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
- Bovie Medical Corporation: 1 (https://510kreport.com/company/bovie-medical)

## Its most-cited devices
- K232805: Kronos Electrocautery Device (2024), cited by 1

## Recent decisions
- K260287: SP Electrocautery Device (SP20) (Feb 24, 2026)
- K232805: Kronos Electrocautery Device (Apr 25, 2024)

Source page: https://510kreport.com/company/single-pass