Pikdare Spa is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Pikdare Spa - FDA 510(k) Cleared Devices
Recent clearances: Insupen Pen needle, Insupen ORIGINAL Pen Needle, Insupen ADVANCED pen needle, DropSafeTM SicuraTM
2
Total
2
Cleared
0
Denied
Pikdare Spa has 2 FDA 510(k) cleared medical devices. Based in Casnate Con Bernate, IT.
Last cleared in 2023. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pikdare Spa Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pikdare Spa
2 devices