Medical Device Manufacturer · US , Fremont , AR

Q'Apel Medical, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2021

Total

Cleared

Denied

Q'Apel Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Fremont, US.

Latest FDA clearance: May 2026. Active since 2021. Primary specialty: Neurology.

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

Regulatory submissions have been managed by Lakeshore Medical Device Consulting, Insight Medical, LLC and Q’Apel Medical, Inc..

Q'Apel Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Q'Apel Medical, Inc.

5 devices

1-5 of 5

Data Source

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

Last updated: Jun 05, 2026