Vesatek, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Vesatek, LLC makes
Vesatek, LLC manufactures wire torque assist devices, including the Firebow and LiteSaber models, designed to facilitate precise torque application during medical procedures.
These Class II devices are listed under the FDA’s 510(k) pathway, reflecting their regulatory clearance in the United States.
Catalogue
Firebow Wire Torque Assist Device Ref K170684
Regimes: 510(k) Registry: 510(k)LiteSaber Wire Torque Assist Device Ref K200120
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vesatek, LLC have in the registry?
The registry currently lists 2 devices for Vesatek, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vesatek, LLC's devices?
Among its 2 most recently registered devices, Vesatek, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Vesatek, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vesatek, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vesatek, LLC in the registry?
The most recently registered devices listed for Vesatek, LLC include Firebow Wire Torque Assist Device and LiteSaber Wire Torque Assist Device.