# Palomar

- Location (FDA's records): Cary, NC
- FDA decisions: 2 (2001–2002): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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
- Cutera, Inc.: 1 (https://510kreport.com/company/cutera)
- Mccue Plc: 1 (https://510kreport.com/company/mccue)
- General Project S.R.L.: 1 (https://510kreport.com/company/general-project)
- Novalis Medical, LLC: 1 (https://510kreport.com/company/novalis-medical)
- Altus Medical, Inc.: 1 (https://510kreport.com/company/altus-medical)
- Aesthera Corporation: 1 (https://510kreport.com/company/aesthera)
- El.En Electronic Engineering Spa: 1 (https://510kreport.com/company/el-en-electronic-engineering)

## Its most-cited devices
- K020941: Palomar Luxg Handpiece (2002), cited by 6
- K010618: Palomar Dermalux Pulsed Light System (2001), cited by 1

## Recent decisions
- K020941: Palomar Luxg Handpiece (Jun 19, 2002)
- K010618: Palomar Dermalux Pulsed Light System (Sep 10, 2001)

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