Biolase, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Biolase, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Irvine, US.
Last cleared in 2022. Active since 2014.
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 Biolase, Inc.
10 devices
Cleared
Apr 21, 2022
Waterlase iPLus
General & Plastic Surgery
451d
Cleared
Dec 22, 2021
EdgePro
Dental
62d
Cleared
Mar 16, 2020
Epic 980
General & Plastic Surgery
90d
Cleared
Dec 04, 2019
Epic 980
General & Plastic Surgery
90d
Cleared
Oct 10, 2019
Waterlase Laser System Family
General & Plastic Surgery
239d
Cleared
Nov 29, 2017
Epic Pro 940
General & Plastic Surgery
76d
Cleared
Jan 11, 2017
Epic Pro
General & Plastic Surgery
64d
Cleared
Jul 28, 2016
Waterlase Express
General & Plastic Surgery
42d
Cleared
Mar 05, 2015
WATERLASE IPLUS S
General & Plastic Surgery
227d
Cleared
Oct 10, 2014
EPIC 10
General & Plastic Surgery
267d