Medical Device Manufacturer · CO , Guarne

New Stetic, SA

2 submissions · 2 cleared · Since 2019
2
Total
2
Cleared
0
Denied

New Stetic, SA — FDA 510(k) Submissions

New Stetic, SA has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Tooth Shade, Resin, Crown And Bridge, Temporary, Resin . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Dental 2