Medical Device Manufacturer · US , Flowery Branch , GA

Gri-Alleset, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2021

Total

Cleared

Denied

Gri-Alleset, Inc. has 4 FDA 510(k) cleared medical devices. Based in Flowery Branch, US.

Latest FDA clearance: Nov 2024. Active since 2021. Primary specialty: General & Plastic Surgery.

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

Regulatory submissions have been managed by Regulatory Resources Group, Inc. and Sterilization Consulting Services, LLC.

FDA 510(k) Regulatory Record - Gri-Alleset, Inc.

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 10, 2026