Luco Hybrid Osa Appliance, Inc. is one of 179 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Luco Hybrid Osa Appliance, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Luco Hybrid Osa Appliance, Inc. has 2 FDA 510(k) cleared medical devices. Based in Kingston, CA.
Historical record: 2 cleared submissions from 2013 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Luco Hybrid Osa Appliance, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luco Hybrid Osa Appliance, Inc.
2 devices