Argomed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Argomed, Inc. makes
Argomed, Inc. manufactures the Thermoflex System, a medical device designed for therapeutic heating applications, likely intended for wound care, pain management, or musculoskeletal therapy.
The Thermoflex System is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Thermoflex System Ref K000508
Regimes: 510(k) Registry: 510(k)Thermoflex System Ref K991847
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Argomed, Inc. have in the registry?
The registry currently lists 2 devices for Argomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Argomed, Inc.'s devices?
Among its 2 most recently registered devices, Argomed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Argomed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Argomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Argomed, Inc. in the registry?
The most recently registered devices listed for Argomed, Inc. include THERMOFLEX SYSTEM.