Techsomed
IsraelFDA applicant, unverified FDA FEI 3030089065
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Techsomed makes
Techsomed manufactures the VisAble.IO, a medical imaging device designed for intraoperative visualization and guidance, likely used in surgical procedures to enhance precision and reduce complications.
The VisAble.IO is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
VisAble.IO Ref K223639
Regimes: 510(k) Registry: 510(k)VisAble.IO Ref K240773
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3030089065
- Address
- 6 Ofra Haza St., Or Yehuda Central
Frequently asked questions
How many devices does Techsomed have in the registry?
The registry currently lists 2 devices for Techsomed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Techsomed's devices?
Among its 2 most recently registered devices, Techsomed has devices listed in FDA 510(k) (2 devices).
What risk classes do Techsomed's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Techsomed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Techsomed in the registry?
The most recently registered devices listed for Techsomed include VisAble.IO.