# Hologic / Gen-Probe Incorporated

- Location (FDA's records): San Diego, CA
- FDA decisions: 1 (2013–2013): 1 510(k) clearance
- Product codes: LSL (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Gen-Probe, Inc.: 1 (https://510kreport.com/company/gen-probe)

## Recent decisions
- K132251: Aptima Combo 2 Assay (Panther System) (Oct 17, 2013)

Source page: https://510kreport.com/company/hologic-gen-probe