Medical Device Manufacturer · US , Naples , FL

Aculux, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Aculux, Inc. has 1 FDA 510(k) cleared medical devices. Based in Naples, US.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: General & Plastic Surgery.

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

1 devices

1–1 of 1