Tactile Medical
Country not established
- Devices
- 3
What Tactile Medical makes
Tactile Medical manufactures the Nimbl (PD08-N1), a portable device designed for airway clearance therapy, and the AffloVest® Mobile, a wearable system for airway clearance at home or during travel.
The company’s products are regulated as Class II devices in the US and are listed under the FDA’s 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Nimbl (model PD08-N1) Ref K234155
Regimes: 510(k) Registry: 510(k)AffloVest® Mobile Airway Clearance Therapy Ref K252849
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tactile Medical have in the registry?
The registry currently lists 3 devices for Tactile Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tactile Medical's devices?
Among its 3 most recently registered devices, Tactile Medical has devices listed in FDA 510(k) (3 devices).
What risk classes do Tactile Medical's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Tactile Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tactile Medical in the registry?
The most recently registered devices listed for Tactile Medical include Flexitouch® Plus Advanced Pneumatic Compression System, Nimbl (model PD08-N1) and AffloVest® Mobile Airway Clearance Therapy.