Cntrl+, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cntrl+, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cntrl+ Bladder Support Pessary
1
Total
1
Cleared
0
Denied
Cntrl+, Inc. has 1 FDA 510(k) cleared medical devices. Based in Cornwall, CA.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cntrl+, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Avania Cro Canada, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cntrl+, Inc.
1 devices