H.B.M. USA Co.,Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
H.B.M. USA Co.,Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
H.B.M. USA Co.,Inc. has 1 FDA 510(k) cleared medical devices. Based in Queen'S Village, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by H.B.M. USA Co.,Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - H.B.M. USA Co.,Inc.
1 devices