# Ra Medical Systems,Inc

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 4 (2007–2022): 4 510(k) clearances
- Product codes: PDU (3), GEX (1)
- Predicates its devices cite: 16 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 7 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Photo Medex, Inc.: 4 (https://510kreport.com/company/photo-medex)
- Lumenis, Inc.: 3 (https://510kreport.com/company/lumenis)
- Surgilight, Inc.: 2 (https://510kreport.com/company/surgilight)
- Theralight, Inc.: 2 (https://510kreport.com/company/theralight)
- Spectranetics Corp.: 1 (https://510kreport.com/company/spectranetics)
- Acculase, Inc.: 1 (https://510kreport.com/company/acculase)
- National Biological Corp.: 1 (https://510kreport.com/company/national-biological)

## Firms that cite its devices most
- Laseroptek Co., Ltd.: 1 (https://510kreport.com/company/laseroptek)

## Its most-cited devices
- K170349: RA-308 Excimer Laser System, Excimer Laser Catheter (2017), cited by 1
- K210664: DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) (2021), cited by 1
- K062963: Pharos Excimer Laser System, Model EX-308 (2007), cited by 1

## Recent decisions
- K220544: DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) (Jun 29, 2022)
- K210664: DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101) (Jul 27, 2021)
- K170349: RA-308 Excimer Laser System, Excimer Laser Catheter (May 24, 2017)
- K062963: Pharos Excimer Laser System, Model EX-308 (Apr 3, 2007)

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