Medical Device Manufacturer · US , Los Angeles , CA

Sprintray, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2021

Total

Cleared

Denied

Sprintray, Inc. has 9 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Latest FDA clearance: Apr 2026. Active since 2021. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Sprintray, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sprintray, Inc.

9 devices

1-9 of 9

SprintRay High Impact Denture Base

K221678 · EBI

Dental · 154d

Cleared Sep 14, 2022

SprintRay Denture Base

Sprintray, Inc. - FDA 510(k) Cleared Devices

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