Fidelity BioPharma Co. is one of 16275 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fidelity BioPharma Co. - FDA 510(k) Cleared Devices
Recent clearances: KCS rTMS Therapy System (Transcranial Magnetic Stimulator) (MetaStim 100, MetaStim 100A)
1
Total
1
Cleared
0
Denied
Fidelity BioPharma Co. has 1 FDA 510(k) cleared medical devices. Based in New Haven, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fidelity BioPharma Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Share Info (Guangzhou) Medical Consultant , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Fidelity BioPharma Co.
1 devices