Usbiomaterials Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Usbiomaterials Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Usbiomaterials Corp. has 5 FDA 510(k) cleared medical devices. Based in Alachua, US.
Historical record: 5 cleared submissions from 1993 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Usbiomaterials Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Usbiomaterials Corp.
5 devices
Cleared
Jul 11, 2003
BUTLER GUM PROPHY PASTE WITH NOVAMIN
Dental
196d
Cleared
Feb 07, 2000
NOVABONE-BIOGLASS BONE GRAFT PARTICULATE
Dental
19d
Cleared
Oct 15, 1999
PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE
Dental
87d
Cleared
Sep 20, 1996
PERIOGLAS - BIOGLASS BONE GRAFT PARTICULATE
Dental
86d
Cleared
Nov 04, 1993
PERIOGLASS
Dental
297d