FindAir Sp. z o.o. is one of 10 FDA 510(k) medical device manufacturers from Poland in the dataset, ranked by real submission volume.
FindAir Sp. z o.o. - FDA 510(k) Cleared Devices
Recent clearances: FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)
1
Total
1
Cleared
0
Denied
FindAir Sp. z o.o. has 1 FDA 510(k) cleared medical devices. Based in Kraków, PL.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by FindAir Sp. z o.o. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pure Global as regulatory consultant.
FDA 510(k) Regulatory Record - FindAir Sp. z o.o.
1 devices