MY01, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
MY01, Inc. has 6 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Latest FDA clearance: Jan 2026. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by MY01, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by MY01, Inc.
6 devices
Cleared
Jan 16, 2026
MY01 Continuous Compartmental Pressure Monitor
Orthopedic
210d
Cleared
Mar 13, 2025
MY01 Continuous Compartmental Pressure Monitor
Orthopedic
168d
Cleared
May 24, 2022
MY01 Continuous Compartmental Pressure Monitor
Orthopedic
53d
Cleared
Apr 22, 2021
MY01 Continuous Compartmental Pressure Monitor
Orthopedic
58d
Cleared
Dec 10, 2020
MY01 Continuous Compartmental Pressure Monitor
Orthopedic
90d
Cleared
Jul 30, 2020
MY01 Continuous Compartmental Pressure Monitor
Orthopedic
241d