Misonix, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
FDA 510(k) cleared devices by Misonix, Inc. General & Plastic Surgery ✕
17 devices
Cleared
Jul 28, 2022
neXus Ultrasonic Surgical Aspirator System
General & Plastic Surgery
90d
Cleared
Dec 13, 2021
neXus Ultrasonic Surgical Aspirator System
General & Plastic Surgery
165d
Cleared
May 30, 2019
neXus Ultrasonic Surgical Aspirator System
General & Plastic Surgery
120d
Cleared
Mar 05, 2013
SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES
General & Plastic Surgery
69d
Cleared
Dec 01, 2011
MISONIX SONICONE(R) ULTRASONIC WOUND CARE SYSTEM AND ACCESSORIES
General & Plastic Surgery
66d
Cleared
Jul 09, 2008
SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM
General & Plastic Surgery
476d
Cleared
May 11, 2007
MISONIX, INC., AUSS-7 ULTRASONIC SURGICAL ASPIRATOR SYSTEM
General & Plastic Surgery
99d
Cleared
Oct 26, 2006
ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RF
General & Plastic Surgery
63d
Cleared
Jan 26, 2006
MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM
General & Plastic Surgery
540d
Cleared
Nov 21, 2005
MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY
General & Plastic Surgery
54d
Cleared
Jun 06, 2005
AUSS-6 ULTRASONIC SURGICAL ASPIRATOR SYSTEM
General & Plastic Surgery
70d
Cleared
May 17, 2004
MISONIX INC. LYSONIX 2000/3000 ULTRASONIC SURGICAL ASPIRATOR SYSTEMS
General & Plastic Surgery
24d