# Geneoscopy, Inc.

- Location (FDA's records): St. Louis
- FDA decisions: 1 (2024–2024): 1 original PMA approval
- Product codes: SBB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- P230001: ColoSense® (May 3, 2024)

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