Remedi, Inc. FDA Approvals

0 new drug approvals and 2 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
REMEX-T(K)100C510(k)Oct 2, 2026Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Oct 2, 2026
REMEX Xcam6510(k)Jul 31, 2025Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jul 31, 2025