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Misonix, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221235neXus Ultrasonic Surgical Aspirator SystemJuly 28, 2022
K212060neXus Ultrasonic Surgical Aspirator SystemDecember 13, 2021
K190160neXus Ultrasonic Surgical Aspirator SystemMay 30, 2019
K123980SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIESMarch 5, 2013
K112782MISONIX SONICONE(R) ULTRASONIC WOUND CARE SYSTEM AND ACCESSORIESDecember 1, 2011
K070779SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEMJuly 9, 2008
K070313MISONIX, INC., AUSS-7 ULTRASONIC SURGICAL ASPIRATOR SYSTEMMay 11, 2007
K062471ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RFOctober 26, 2006
K042096MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEMJanuary 26, 2006
K052702MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORYNovember 21, 2005
K050776AUSS-6 ULTRASONIC SURGICAL ASPIRATOR SYSTEMJune 6, 2005
K041058MISONIX INC. LYSONIX 2000/3000 ULTRASONIC SURGICAL ASPIRATOR SYSTEMSMay 17, 2004
K032690MISONIX INC. FS 1000 RF ULTRASONIC SURGICAL ASPIRATOR SYSTEMDecember 9, 2003
K013417MISONIX IRRIGATION SYSTEM MOEDL BC20PJanuary 10, 2002
K012028ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-5July 27, 2001
K000927ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-4October 10, 2000
K982841MODIFICATION TO ALLIGER ULTRASONIC SURGICAL SYSTEM, MODEL AUSS-4September 4, 1998