# Preswede AB

- Location (FDA's records): Great Neck, NY
- FDA decisions: 2 (2003–2004): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)
- Esc Medical Systems, Ltd.: 1 (https://510kreport.com/company/esc-medical-systems)

## Its most-cited devices
- K030423: Powerlite 600 EP System (2003), cited by 1

## Recent decisions
- K033933: Powerlite 600 EX System (Mar 16, 2004)
- K030423: Powerlite 600 EP System (May 9, 2003)

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