Premier North America, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Premier North America, Inc. has 6 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.
Latest FDA clearance: Mar 2024. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Premier North America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Premier North America, Inc.
6 devices
Cleared
Mar 01, 2024
NUNA LUX (NUNL528)
General & Plastic Surgery
86d
Cleared
Nov 14, 2023
BLU TOTALE (Model: ENEOB852)
General & Plastic Surgery
75d
Cleared
Sep 15, 2023
Avologi Gel Primer (Model: Av25)
Neurology
550d
Cleared
Feb 24, 2022
Luminice
Neurology
57d
Cleared
Jan 06, 2022
ENEO TOTALE (Model: ENEOT947)
General & Plastic Surgery
28d
Cleared
Jul 26, 2018
Avologi ENEO
General & Plastic Surgery
31d