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) cleared devices by Avery Dennison Belgie Bvba

5 devices

1-5 of 5