Sprintray, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250617Apex FlexApril 29, 2025
K242559Digital TempNovember 26, 2024
K242277Crown HTOctober 1, 2024
K230445OnX ToughJuly 14, 2023
K222623Digital CrownDecember 14, 2022
K221678SprintRay High Impact Denture BaseNovember 10, 2022
K220979SprintRay Denture BaseSeptember 14, 2022
K212448NightGuard FlexNovember 12, 2021