Konica Minolta, Inc. FDA Approvals

0 new drug approvals and 10 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
SKR 3000510(k)Jun 17, 2025Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jun 17, 2025
SKR 3000510(k)Nov 21, 2024Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Nov 21, 2024
Bone Suppression Software510(k)May 31, 2024Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	May 31, 2024
Konicaminolta DI-X1510(k)Apr 25, 2023Radiology	Radiology	510(k)Substantially Equivalent (Special)	Apr 25, 2023
SKR 3000510(k)Nov 17, 2022Radiology	Radiology	510(k)Substantially Equivalent (Special)	Nov 17, 2022
Ultrasound System SONIMAGE MX1510(k)Jun 23, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jun 23, 2022
SKR 3000510(k)Jan 31, 2022Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Jan 31, 2022
KONICAMINOLTA DI-X1510(k)Sep 13, 2021Radiology	Radiology	510(k)Substantially Equivalent (Special)	Sep 13, 2021
SKR 3000510(k)Aug 24, 2021Radiology	Radiology	510(k)Substantially Equivalent (Traditional)	Aug 24, 2021
ImagePilot510(k)May 6, 2021Radiology	Radiology	510(k)Substantially Equivalent (Special)	May 6, 2021