ArthroCare Corporation - FDA 510(k) Cleared Devices
Recent clearances: LYNX COBLATION Laryngeal Wand (72290254), FLOW 90? Wand, INTELLIO SHIFT System
36
Total
36
Cleared
0
Denied
FDA 510(k) Regulatory Record - ArthroCare Corporation General & Plastic Surgery ✕
22 devices
Cleared
Mar 25, 2026
LYNX COBLATION Laryngeal Wand (72290254)
General & Plastic Surgery
124d
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
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