# Progene Corp.

- Location (FDA's records): Overland Park, KS
- FDA decisions: 3 (1988–1989): 3 510(k) clearances
- Product codes: DGC (1), JIR (1), DHB (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K895294: Progene Ige Bead Eia (Sep 21, 1989)
- K882538: Progene Microalbuminuria Screen (Mar 13, 1989)
- K875125: Progene (TM) Ige Test (Feb 25, 1988)

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