Resnent, LLC
Country not established
- Devices
- 1
What Resnent, LLC makes
Resnent, LLC manufactures the Outlook Surgical Versa One System, a surgical device designed for precise tissue manipulation and dissection during minimally invasive procedures.
The company’s portfolio is regulated under FDA Class II devices, with the Versa One System authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Outlook Surgical Versa One System (8900139) Ref K241731
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Resnent, LLC have in the registry?
The registry currently lists 1 device for Resnent, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Resnent, LLC's devices?
Among its 1 most recently registered device, Resnent, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Resnent, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Resnent, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Resnent, LLC in the registry?
The most recently registered devices listed for Resnent, LLC include Outlook Surgical Versa One System (8900139).