# Luma Vision Limited

- Location (FDA's records): Dublin, IE
- FDA decisions: 3 (2025–2026): 3 510(k) clearances
- Product codes: OBJ (2)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 2 (2 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
- Siemens Medical Solutions USA, Inc.: 2 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Abbott Medical: 1 (https://510kreport.com/company/abbott-medical)

## Its most-cited devices
- K242893: VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System (2025), cited by 2

## Recent decisions
- K261849: VERAFEYE Imaging Catheter (VF-VIC-002) (Jul 24, 2026)
- K260885: VERAFEYE Imaging and Guidance System (VF-VIS-002) (Jun 15, 2026)
- K242893: VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System (Mar 24, 2025)

Source page: https://510kreport.com/company/luma-vision