# Laurus Medical Corp.

- Location (FDA's records): Irvine, CA
- FDA decisions: 4 (1994–1997): 4 510(k) clearances
- Product codes: GCJ (2), FCG (1), KNW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Louisville Laboratories, Inc.: 3 (https://510kreport.com/company/louisville-laboratories)

## Its most-cited devices
- K932553: Disposable Suture Placement System (1994), cited by 3

## Recent decisions
- K973415: Curvilinear Suture Placement System (Dec 2, 1997)
- K973215: Stereotactic Needle Core Biopsy System (Nov 6, 1997)
- K960317: Laurus Needle Core Biopsy System (Mar 15, 1996)
- K932553: Disposable Suture Placement System (May 12, 1994)

Source page: https://510kreport.com/company/laurus-medical