Osspray, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osspray, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Osspray, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Gainesville, US.
Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osspray, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osspray, Ltd.
2 devices