Avita Corporation

FDA Regulatory Profile

Avita Corporation appears in FDA public data with 0 recalls, 27 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 11, 2026.

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250129AViTA Breast PumpJun 11, 2026
K252448AViTA Pulse Oximeter (SP61)Feb 27, 2026
K250765AViTA Arm Type Blood Pressure Monitor CuffSep 3, 2025
K242455AViTA Pulse Oximeter (SP62B)Feb 19, 2025
K241852Nasal Aspirator (NS 13)Dec 31, 2024
K242193Arm Type Blood Pressure Monitor (BPM82)Oct 22, 2024
K223399AViTA Pulse OximeterMay 20, 2024
K200346Wrist Type Blood Pressure MonitorDec 17, 2020
K180155Arm Type Blood Pressure MonitorAug 3, 2018
K172427AViTA Radar Thermo NT16 Series IR ThermometerApr 19, 2018
K112825AVITA ARM TYPE BLOOD PRESSURE MONITORJan 18, 2012
K110559AVITA INFRARED THEROMETER WITH BLUETOOTHJan 6, 2012
K102554AVITA SCANEO IR THERMOMETER MODEL TS4X SERIESMar 3, 2011
K102624AVITA WRIST TYPE BLOOD PRESSURE MONITORDec 16, 2010
K090379AVITA NASAL ASPIRATOR, MODEL, NS1 SERIESMay 26, 2010
K100016AVITA SCANEO INFRARED EAR THERMOMETER, MODEL TS7Mar 4, 2010
K092958AVITA SCANEO IR THERMOMETER, MODELS TS2X & TS3X SERIESDec 2, 2009
K092959AVITA RADAR THERMO IR THERMOMETER, MODEL NT 152Nov 27, 2009
K081160AVITA RADAR THERMO IR THERMOMETER, NT1 SERIESJun 24, 2008
K072137AVITA BLUETOOTH BLOOD PRESSURE MONITOR, MODEL: BPM656ZBDec 7, 2007