Allergan is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Allergan has 5 FDA 510(k) cleared medical devices. Based in Medford, US.
Last cleared in 2021. Active since 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Allergan Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allergan
6 devices
Cleared
Jun 02, 2021
NATRELLE INSPIRA Single Use Sizers for Gel Implants
General & Plastic Surgery
212d
Cleared
Aug 31, 2020
TrueTear Intranasal Tear Neurostimulator
Ophthalmic
252d
Cleared
Dec 21, 2018
Natrelle 133 Plus MICROCELL Tissue Expander
General & Plastic Surgery
266d
Cleared
Aug 29, 2018
Natrelle 133S Tissue Expander
General & Plastic Surgery
29d
Not Cleared
May 17, 2018
TrueTear Intranasal Tear Neurostimulator
Ophthalmic
206d
Cleared
Apr 25, 2013
SERI SURGICAL SCAFFOLD
General & Plastic Surgery
203d