Viatherm Therapeutics, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Viatherm Therapeutics, LLC makes
Viatherm Therapeutics, LLC manufactures the ViVY, a non-invasive, wearable device designed for targeted hyperthermia therapy, and the ViaTherm BOOST, a system for localized temperature-controlled treatments. These products are intended for medical applications requiring controlled heat delivery to specific tissues or regions.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. Both devices are listed in the FDA’s 510(k) premarket notification database. The manufacturer is based in the United States.
Catalogue
ViVY Ref K250376
Regimes: 510(k) Registry: 510(k)ViaTherm BOOST Ref K173300
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viatherm Therapeutics, LLC have in the registry?
The registry currently lists 2 devices for Viatherm Therapeutics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viatherm Therapeutics, LLC's devices?
Among its 2 most recently registered devices, Viatherm Therapeutics, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Viatherm Therapeutics, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Viatherm Therapeutics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viatherm Therapeutics, LLC in the registry?
The most recently registered devices listed for Viatherm Therapeutics, LLC include ViVY and ViaTherm BOOST.