Medical Device Manufacturer · US , Painesville , OH

Avery Intl. - FDA 510(k) Cleared Devices

12 submissions · 6 cleared · Since 1986
12
Total
6
Cleared
0
Denied

Avery Intl. has 6 FDA 510(k) cleared medical devices. Based in Painesville, US.

Historical record: 6 cleared submissions from 1986 to 1987. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Avery Intl.

12 devices
1-12 of 12
Filters