Medical Device Manufacturer · US , Jacksonville , FL

Anjon Holdings, LLC

2 submissions · 2 cleared · Since 2018
2
Total
2
Cleared
0
Denied

Anjon Holdings, LLC — FDA 510(k) Submissions

Anjon Holdings, LLC has submitted 2 FDA 510(k) premarket notifications since 2018, of which 2 received clearance as substantially equivalent to a predicate device.

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

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Orthopedic 2