Telios Pharmaceuticals, Inc.
Country not established
- Devices
- 1
What Telios Pharmaceuticals, Inc. makes
Telios Pharmaceuticals, Inc. manufactures ARGIDENE™ GEL, a topical gel designed for wound care applications.
ARGIDENE™ GEL is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Argidene(Tm) Gel Ref K945835
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telios Pharmaceuticals, Inc. have in the registry?
The registry currently lists 1 device for Telios Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telios Pharmaceuticals, Inc.'s devices?
Among its 1 most recently registered device, Telios Pharmaceuticals, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Telios Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Telios Pharmaceuticals, Inc. include ARGIDENE(TM) GEL.