# Medart A/S

- Location (FDA's records): Hvidovre, DK
- FDA decisions: 3 (2009–2012): 3 510(k) clearances
- Product codes: GEX (3)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Medart Corp.: 1 (https://510kreport.com/company/medart)
- Biolitec, Inc.: 1 (https://510kreport.com/company/biolitec)

## Recent decisions
- K120573: Medart 620 (Jun 13, 2012)
- K110243: Medart Diode Laser System & Accessories (Jun 28, 2011)
- K083123: Medart Model 610 CO2 Laser System & Accessories (Nov 24, 2009)

Source page: https://510kreport.com/company/medart-a-s