Neoss Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Neoss Limited - FDA 510(k) Cleared Devices
Recent clearances: Membrane Screws and Membrane Tacks
1
Total
1
Cleared
0
Denied
Neoss Limited has 1 FDA 510(k) cleared medical devices. Based in Harrogate, GB.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Neoss Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neoss Limited
1 devices