# Lca, Inc.

- Location (FDA's records): Cincinnati, OH
- FDA decisions: 12 (1990–1995): 12 510(k) clearances
- Product codes: GEX (10), FYD (1), GEI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Slt-J, Ltd.: 5 (https://510kreport.com/company/slt-j)

## Its most-cited devices
- K924120: Molded Fiber Cap Delivery System (1993), cited by 1
- K901365: Laser Forceps Handpiece (1990), cited by 1
- K923991: Zoe Laser, Contact ND:Yag Laser System (1993), cited by 1
- K924160: Hybrid Surgical Device (1993), cited by 1
- K931070: Closed End Fiberoptic Laser Delivery System (1993), cited by 1

## Recent decisions
- K952792: Padless Electrosurgical Pencil (Aug 28, 1995)
- K944091: The Hook-Curved Closed End/Elect Fiber Laser Deliv Sys (Oct 7, 1994)
- K935439: SNJ Smoke Evacuation Suction Wand (Mar 7, 1994)
- K935258: Hybrid Surgical Device Modification (Jan 13, 1994)
- K925726: Alloy Scalpel Handpieces, Modification (Nov 22, 1993)
- K931070: Closed End Fiberoptic Laser Delivery System (Oct 5, 1993)
- K924160: Hybrid Surgical Device (Apr 23, 1993)
- K923991: Zoe Laser, Contact ND:Yag Laser System (Mar 31, 1993)

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