Medical Device Manufacturer · US , Austin , TX

Alafair Biosciences

3 submissions · 3 cleared · Since 2025
3
Total
3
Cleared
0
Denied

Alafair Biosciences — FDA 510(k) Submissions

Alafair Biosciences has submitted 3 FDA 510(k) premarket notifications since 2025, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cuff, Nerve, Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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