Exsomed Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Exsomed Corp. - FDA 510(k) Cleared Devices
Recent clearances: ExsoMed INnate NanoTM Lag Screw System, InFrame™ Cannulated Fixation System
2
Total
2
Cleared
0
Denied
Exsomed Corp. has 2 FDA 510(k) cleared medical devices. Based in Aliso Viejo, US.
Last cleared in 2022. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Exsomed Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory and Quality Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Exsomed Corp.
2 devices