ArthroCare Corporation - FDA 510(k) Cleared Devices
35
Total
35
Cleared
0
Denied
ArthroCare Corporation has 35 FDA 510(k) cleared medical devices. Based in Irvine, US.
Latest FDA clearance: May 2024. Active since 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by ArthroCare Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by ArthroCare Corporation
35 devices
Cleared
May 08, 2024
FLOW 90? Wand
General & Plastic Surgery
29d
Cleared
Dec 11, 2023
INTELLIO SHIFT System
General & Plastic Surgery
132d
Cleared
Jun 26, 2023
ARIS¿ COBLATION¿ Turbinate Reduction Wand (72290113)
General & Plastic Surgery
87d
Cleared
Sep 01, 2022
Ambient HipVac 50 Wand with Integrated Finger Switches, RF20000 COBLATION...
General & Plastic Surgery
185d
Cleared
Jun 24, 2021
Werewolf+ Coblation System, Werewolf+ Controller, Werewolf Fastseal 6.0...
General & Plastic Surgery
133d
Cleared
Dec 18, 2020
ENT Plasma Wands, Turbinator Wand, Werewolf Irrigation Tube Set, Werewolf ENT...
General & Plastic Surgery
150d
Cleared
Dec 20, 2019
WEREWOLF COBLATION System, COBLATION HALO Wand
General & Plastic Surgery
144d
Cleared
Jan 24, 2019
FLOW 90 Wand
General & Plastic Surgery
52d
Cleared
May 01, 2018
AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches
General & Plastic Surgery
29d
Cleared
Aug 17, 2017
Q-Fix Suture Anchor
Orthopedic
30d
Cleared
Jan 06, 2017
SpeedStitch Suture Passer
General & Plastic Surgery
58d
Cleared
Oct 21, 2016
Ambient HipVac 50 Wand with Integrated Finger Switches
General & Plastic Surgery
143d