Minitube AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Minitube AB - FDA 510(k) Cleared Devices
Recent clearances: Minitube Dentasleeve Protective Barrier Sleeves
1
Total
1
Cleared
0
Denied
Minitube AB has 1 FDA 510(k) cleared medical devices. Based in Tr?ngsviken, SE.
Last cleared in 2021. Active since 2021. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Minitube AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Minitube AB
1 devices