Microlife Corporation is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Microlife Corporation - FDA 510(k) Cleared Devices
Recent clearances: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP Progress (BP3T01-1B)
3
Total
3
Cleared
0
Denied
Microlife Corporation has 3 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Latest FDA clearance: Jul 2026. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Microlife Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microlife Corporation
3 devices
Cleared
Jul 23, 2026
Microlife Wrist Blood Pressure Monitor , (Model BPHJG5-G)
Cardiovascular
113d
Cleared
Jun 23, 2026
Microlife Digital Peak Flow Meter, Model PF200B (PF200B)
Anesthesiology
270d
Cleared
Aug 06, 2025
Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP...
Cardiovascular
117d