Medical Device Manufacturer · US , Raleigh , NC

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

2 submissions · 2 cleared · Since 2025

Total

Cleared

Denied

Staclear, Inc. has 2 FDA 510(k) cleared medical devices. Based in Raleigh, US.

Latest FDA clearance: Nov 2025. Active since 2025. Primary specialty: General Hospital.

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

Staclear, 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 - Staclear, Inc.

2 devices

1-2 of 2