Biofourmis Singapore Pte., Ltd. is one of 29 FDA 510(k) medical device manufacturers from Singapore in the dataset, ranked by real submission volume.
Biofourmis Singapore Pte., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Biofourmis Everion+ (G2), Everion+ System, Biovitals Analytics Engine
4
Total
4
Cleared
0
Denied
Biofourmis Singapore Pte., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Singapore, SG.
Latest FDA clearance: May 2024. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Biofourmis Singapore Pte., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Daniel & Daniel Consulting, LLC and Rakesh Lal. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Biofourmis Singapore Pte., Ltd.
4 devices