Okami Medical, Inc. FDA Approvals

0 new drug approvals and 4 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
LOBO Vascular Occlusion System510(k)Apr 10, 2026Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Apr 10, 2026
SENDERO MAX Delivery Catheter510(k)Dec 20, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Dec 20, 2024
SENDERO Microcatheter510(k)Mar 8, 2024Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Special)	Mar 8, 2024
SENDERO Microcatheter510(k)Nov 17, 2023Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Nov 17, 2023