Qualimed Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Qualimed Srl - FDA 510(k) Cleared Devices
Recent clearances: Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted)
2
Total
2
Cleared
0
Denied
Qualimed Srl has 2 FDA 510(k) cleared medical devices. Based in Rome, IT.
Historical record: 2 cleared submissions from 2014 to 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Qualimed Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Qualimed Srl
2 devices