Medical Device Manufacturer · US , Chicago , IL

Avery Dennison Belgie Bvba - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Total

Cleared

Denied

Avery Dennison Belgie Bvba has 5 FDA 510(k) cleared medical devices. Based in Chicago, US.

Last cleared in 2021. Active since 2012. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Avery Dennison Belgie Bvba Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Avery Dennison Belgie Bvba

5 devices

1-5 of 5

Data Source

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

Last updated: May 23, 2026