Misonix, Inc.
Misonix, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2022.
Top product codes for Misonix, Inc.
Recent clearances by Misonix, Inc.
- K221235 — neXus Ultrasonic Surgical Aspirator System
- K212060 — neXus Ultrasonic Surgical Aspirator System
- K190160 — neXus Ultrasonic Surgical Aspirator System
- K123980 — SONICONE PLUS ULTRASOUND WOUND CARE SYSTEM AND ACCESSORIES
- K112782 — MISONIX SONICONE(R) ULTRASONIC WOUND CARE SYSTEM AND ACCESSORIES
- K070779 — SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM
- K070313 — MISONIX, INC., AUSS-7 ULTRASONIC SURGICAL ASPIRATOR SYSTEM
- K062471 — ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RF
- K042096 — MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM
- K052702 — MISONIX INC. FS-1000-RF BIPOLAR FORCEPS ACCESSORY
- K050776 — AUSS-6 ULTRASONIC SURGICAL ASPIRATOR SYSTEM
- K041058 — MISONIX INC. LYSONIX 2000/3000 ULTRASONIC SURGICAL ASPIRATOR SYSTEMS
- K032690 — MISONIX INC. FS 1000 RF ULTRASONIC SURGICAL ASPIRATOR SYSTEM
- K013417 — MISONIX IRRIGATION SYSTEM MOEDL BC20P
- K012028 — ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-5
- K000927 — ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-4
- K982841 — MODIFICATION TO ALLIGER ULTRASONIC SURGICAL SYSTEM, MODEL AUSS-4
Data sourced from openFDA. This site is unofficial and independent of the FDA.