Medical Device Manufacturer · US , Elk Grove Village , IL

Headstart, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021

Recent clearances: SnugKap

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Headstart, Ltd. Neurology ✕

1 devices

1-1 of 1

Cleared Jun 07, 2021

Neurology · 550d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 25, 2026