Tactile Systems Technology, Inc. (Dba Tactile Medical)
United StatesFDA applicant, unverified
- Devices
- 3
What Tactile Systems Technology, Inc. (Dba Tactile Medical) makes
Tactile Systems Technology, Inc. manufactures the Flexitouch Plus System and Flexitouch System, which are designed for tactile feedback in medical training and simulation environments. These systems provide haptic feedback to enhance procedural training, particularly for surgical and interventional techniques.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Flexitouch Plus System Ref K203178
Regimes: 510(k) Registry: 510(k)Flexitouch System Ref K153311
Regimes: 510(k) Registry: 510(k)Flexitouch System Ref K170216
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tactile Systems Technology, Inc. (Dba Tactile Medical) have in the registry?
The registry currently lists 3 devices for Tactile Systems Technology, Inc. (Dba Tactile Medical). Devices recorded under merged duplicate company entries are counted once.
Which registries list Tactile Systems Technology, Inc. (Dba Tactile Medical)'s devices?
Among its 3 most recently registered devices, Tactile Systems Technology, Inc. (Dba Tactile Medical) has devices listed in FDA 510(k) (3 devices).
What risk classes do Tactile Systems Technology, Inc. (Dba Tactile Medical)'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Tactile Systems Technology, Inc. (Dba Tactile Medical)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tactile Systems Technology, Inc. (Dba Tactile Medical) in the registry?
The most recently registered devices listed for Tactile Systems Technology, Inc. (Dba Tactile Medical) include Flexitouch Plus System and Flexitouch System.