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.

Avery Dennison Belgie Bvba 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 - Avery Dennison Belgie Bvba

5 devices

1-5 of 5

Data Source

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

Last updated: May 23, 2026