Mesi D.O.O. is one of 8 FDA 510(k) medical device manufacturers from Slovenia in the dataset, ranked by real submission volume.
Mesi D.O.O. - FDA 510(k) Cleared Devices
Recent clearances: MESI mTABLET SPIRO
1
Total
1
Cleared
0
Denied
Mesi D.O.O. has 1 FDA 510(k) cleared medical devices. Based in Ljubljana, SI.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Mesi D.O.O. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mesi D.O.O.
1 devices