# Medart Corp.

- Location (FDA's records): San Diego, CA
- FDA decisions: 5 (1999–2001): 5 510(k) clearances
- Product codes: GEX (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (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
- Vascular Solutions, Inc.: 2 (https://510kreport.com/company/vascular-solutions)
- Lumenis, Inc.: 2 (https://510kreport.com/company/lumenis)
- Opusdent, Ltd.: 1 (https://510kreport.com/company/opusdent)
- Reliant Technologies, Inc.: 1 (https://510kreport.com/company/reliant-technologies)
- Medart A/S: 1 (https://510kreport.com/company/medart-a-s)
- Max Engineering, Ltd.: 1 (https://510kreport.com/company/max-engineering)
- Arthrocare Corp.: 1 (https://510kreport.com/company/arthrocare)
- Lutronic Corporation: 1 (https://510kreport.com/company/lutronic)

## Its most-cited devices
- K991297: Uni-Laser 450P CO2 Laser System & Accessories (1999), cited by 6
- K000503: Medart 520 Cooling System (2000), cited by 2
- K993815: Uni-Laser 430 (2000), cited by 1
- K991659: Uni-Laser 425P Diode Laser System & Accessories (1999), cited by 1

## Recent decisions
- K010885: Uni-Laser 470 (Jun 7, 2001)
- K000503: Medart 520 Cooling System (May 15, 2000)
- K993815: Uni-Laser 430 (May 11, 2000)
- K991659: Uni-Laser 425P Diode Laser System & Accessories (Jul 29, 1999)
- K991297: Uni-Laser 450P CO2 Laser System & Accessories (Jul 12, 1999)

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