Sprintray, Inc. FDA Approvals

0 new drug approvals and 9 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
Midas Restore510(k)Apr 15, 2026Dental	Dental	510(k)Substantially Equivalent (Traditional)	Apr 15, 2026
Apex Flex510(k)Apr 29, 2025Dental	Dental	510(k)Substantially Equivalent (Traditional)	Apr 29, 2025
Digital Temp510(k)Nov 26, 2024Dental	Dental	510(k)Substantially Equivalent (Traditional)	Nov 26, 2024
Crown HT510(k)Oct 1, 2024Dental	Dental	510(k)Substantially Equivalent (Traditional)	Oct 1, 2024
OnX Tough510(k)Jul 14, 2023Dental	Dental	510(k)Substantially Equivalent (Traditional)	Jul 14, 2023
Digital Crown510(k)Dec 14, 2022Dental	Dental	510(k)Substantially Equivalent (Traditional)	Dec 14, 2022
SprintRay High Impact Denture Base510(k)Nov 10, 2022Dental	Dental	510(k)Substantially Equivalent (Traditional)	Nov 10, 2022
SprintRay Denture Base510(k)Sep 14, 2022Dental	Dental	510(k)Substantially Equivalent (Traditional)	Sep 14, 2022
NightGuard Flex510(k)Nov 12, 2021	—	510(k)Substantially Equivalent (Traditional)	Nov 12, 2021