Medical Device Manufacturer · US , Chatham , NJ

Lone Star Technologies

2 submissions · 2 cleared · Since 1998
2
Total
2
Cleared
0
Denied

Lone Star Technologies — FDA 510(k) Submissions

Lone Star Technologies has submitted 2 FDA 510(k) premarket notifications since 1998, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Handle, Instrument, Dental, Material, Impression . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Dental 2