# Laser Center Dev. Corp.

- Location (FDA's records): St. Louis, MO
- FDA decisions: 2 (1998–1998): 2 510(k) clearances
- Product codes: HRG (1), HNC (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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 whose devices it cites most
- Precision Instruments, Inc.: 1 (https://510kreport.com/company/precision-instruments)
- Eyefix, Inc.: 1 (https://510kreport.com/company/eyefix)

## Firms that cite its devices most
- Lensx Lasers, Inc.: 1 (https://510kreport.com/company/lensx-lasers)
- Intra Lase Corp.: 1 (https://510kreport.com/company/intra-lase)

## Its most-cited devices
- K981063: Automated Corneal Trephine (1998), cited by 2

## Recent decisions
- K981235: Oculostat (Jul 15, 1998)
- K981063: Automated Corneal Trephine (Jun 23, 1998)

Source page: https://510kreport.com/company/laser-center-dev