Respiree Pte, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Respiree Pte, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Singapore, SG.
Latest FDA clearance: Aug 2025. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Respiree Pte, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Msquared Associates, Inc. and Propharma Group.
2 devices