Tactile Systems Technology, Inc. (Dba Tactile Medical) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tactile Systems Technology, Inc. (Dba Tactile Medical) - FDA 510(k) C...
Recent clearances: Flexitouch Plus System
3
Total
3
Cleared
0
Denied
Tactile Systems Technology, Inc. (Dba Tactile Medical) has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 3 cleared submissions from 2016 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tactile Systems Technology, Inc. (Dba Tactile Medical) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The Tamarack Group – Mpls, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tactile Systems Technology, Inc. (Dba Tactile Medical)
3 devices