Konica Minolta Healthcare Americas, Inc. 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
Universal 1417PI510(k)Jun 12, 2026Radiology	Radiology	510(k)Substantially Equivalent (Abbreviated)	Jun 12, 2026
OTC DDR510(k)Jul 27, 2022Radiology	Radiology	510(k)Substantially Equivalent (Special)	Jul 27, 2022
Universal DR 1748510(k)Jan 21, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jan 21, 2022
Straight Arm DDR510(k)Jan 12, 2022Radiology	Radiology	510(k)Substantially Equivalent (Special)	Jan 12, 2022
EXA510(k)Dec 10, 2021Radiology	Radiology	510(k)Substantially Equivalent (Special)	Dec 10, 2021