Arbor Endovascular, LLC FDA Approvals

0 new drug approvals and 5 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
Willow 12 Guidewire510(k)Aug 14, 2026Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Special)	Aug 14, 2026
Willow 24 Guidewire510(k)Mar 19, 2026Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Special)	Mar 19, 2026
Willow 18 Guidewire510(k)Feb 13, 2026Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Special)	Feb 13, 2026
0.014 Willow Guidewire510(k)Nov 26, 2025Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Special)	Nov 26, 2025
0.014 Willow Guidewire510(k)Jul 17, 2025Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Jul 17, 2025