# Coopervision Surgical

- Location (FDA's records): Trumbull
- FDA decisions: 3 (1975–1992): 2 510(k) clearances and 1 original PMA approval
- Product codes: LTA (1), GCT (1), HGI (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
- K921390: Xenon Light Source and Accessories (Jul 27, 1992)
- K905747: Leep System 6000 Electrosurgical Unit and Accessor (Sep 17, 1991)
- N17511: Hyskon (32% Dextran 70) (Sep 15, 1975)

Source page: https://510kreport.com/company/coopervision-surgical