Allergan - FDA 510(k) Cleared Devices
Recent clearances: NATRELLE INSPIRA Single Use Sizers for Gel Implants, TrueTear Intranasal Tear Neurostimulator, Natrelle 133 Plus MICROCELL Tissue Expander
6
Total
5
Cleared
1
Denied
FDA 510(k) Regulatory Record - Allergan Ophthalmic ✕
2 devices