Medical Device Manufacturer · CH , Renens

Aspivix SA

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Aspivix SA — FDA 510(k) Submissions

Aspivix SA has submitted 2 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tenaculum, Uterine . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Obstetrics & Gynecology 2