Mauna Kea Technologies - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Mauna Kea Technologies has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Paris, FR.
Last cleared in 2022. Active since 2005.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mauna Kea Technologies
18 devices
Cleared
Apr 11, 2022
Cellvizio 100 series system with confocal Miniprobes
General & Plastic Surgery
52d
Cleared
Aug 18, 2021
Cellvizio I.V.E. system with Confocal Miniprobes
General & Plastic Surgery
23d
Cleared
Feb 28, 2020
Cellvizio I.V.E. with Confocal Miniprobes
General & Plastic Surgery
81d
Cleared
Jan 24, 2020
Cellvizio 100 Series System with Confocal Miniprobes
General & Plastic Surgery
269d
Cleared
Feb 22, 2019
Cellvizio 100 Series Confocal laser Imaging systems and their Confocal...
General & Plastic Surgery
58d
Cleared
May 22, 2018
Cellvizio 100 Series Systems with Confocal Miniprobes
Neurology
111d
Cleared
Dec 15, 2017
Cellvizio 100 Series System with Confocal Miniprobes
General & Plastic Surgery
87d
Cleared
Aug 04, 2017
Cellvizio 100 Series Systems with Confocal Miniprobes
General & Plastic Surgery
88d
Cleared
May 20, 2016
CystoFlex UHD R-C, CelioFlex UHD 5-C, Cellvizio 100 Series (800) with...
General & Plastic Surgery
94d
Cleared
Dec 22, 2015
Cellvizio 100 Series System with Confocal Miniprobes
General & Plastic Surgery
267d
Cleared
Oct 23, 2015
Cellvizio 100 Series System with Confocal Miniprobes
General & Plastic Surgery
133d
Cleared
Sep 25, 2014
CELLVIZIO 100 SERIES WITH SYSTEM CONFOCAL MINIPROBES
General & Plastic Surgery
125d