Misonix, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Misonix, Inc. has 17 FDA 510(k) cleared general & plastic surgery devices. Based in Farmingdale, US.
Last cleared in 2022. Active since 1998.
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 Misonix, Inc.
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