Fit-Pro KFT (Ltd.) - DBA E-Fit is one of 11 FDA 510(k) medical device manufacturers from Hungary in the dataset, ranked by real submission volume.
Fit-Pro KFT (Ltd.) - DBA E-Fit - FDA 510(k) Cleared Devices
Recent clearances: Ultima System (UL-800)
1
Total
1
Cleared
0
Denied
Fit-Pro KFT (Ltd.) - DBA E-Fit has 1 FDA 510(k) cleared medical devices. Based in Budapest, HU.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Fit-Pro KFT (Ltd.) - DBA E-Fit Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Fit-Pro KFT (Ltd.) - DBA E-Fit
1 devices