Altex Vision
Country not established
- Devices
- 2
What Altex Vision makes
Altex Vision manufactures disposable and reusable vitrectomy probes, which are surgical instruments used to remove the vitreous humor from the eye during vitreoretinal procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Disposable Vitrectomy Probe Ref K970673
Regimes: 510(k) Registry: 510(k)Reusable Vitrectomy Probe Ref K970670
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Altex Vision have in the registry?
The registry currently lists 2 devices for Altex Vision. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altex Vision's devices?
Among its 2 most recently registered devices, Altex Vision has devices listed in FDA 510(k) (2 devices).
What risk classes do Altex Vision's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Altex Vision's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altex Vision in the registry?
The most recently registered devices listed for Altex Vision include DISPOSABLE VITRECTOMY PROBE and REUSABLE VITRECTOMY PROBE.