Respiree Pte, Ltd. is one of 29 FDA 510(k) medical device manufacturers from Singapore in the dataset, ranked by real submission volume.
Respiree Pte, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Respiree Cardio- Respiratory Monitor System, Respiree Cardio-Respiratory Monitor
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.
FDA 510(k) Regulatory Record - Respiree Pte, Ltd.
2 devices