Freyja Healthcare, LLC FDA Approvals

0 new drug approvals and 3 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
VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)510(k)Aug 13, 2026Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Aug 13, 2026
VereSee Optical Veres Needle and Endoscopic Camera510(k)Oct 20, 2025Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Oct 20, 2025
VereSee Optical Veres Needle System510(k)May 2, 2024Obstetrics/Gynecology	Obstetrics/Gynecology	510(k)Substantially Equivalent (Traditional)	May 2, 2024