# Qualimed Srl

- Location (FDA's records): Rome, IT
- FDA decisions: 2 (2014–2018): 2 510(k) clearances
- Product codes: LPL (2)
- 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
- Vision Science Co., Ltd.: 1 (https://510kreport.com/company/vision-science)
- Hydrogel Vision Corporation: 1 (https://510kreport.com/company/hydrogel-vision)

## Recent decisions
- K181050: Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) (Jun 13, 2018)
- K142384: DESIO (polymacon) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted) (Dec 12, 2014)

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