Hans Biomed Corp. is one of 18461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hans Biomed Corp. - FDA 510(k) Cleared Devices
Recent clearances: MaxiGen, BellaFuse, SURFUSE II GEL, SURFUSE II PUTTY, EXFUSE II GEL, EXFUSE II PUTTY
4
Total
4
Cleared
0
Denied
Hans Biomed Corp. has 4 FDA 510(k) cleared medical devices. Based in Chevy Chase, US.
Historical record: 4 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hans Biomed Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Trisler Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Hans Biomed Corp.
4 devices