Medical Device Manufacturer · US , Northbrook , IL

Aeros Instruments, Inc. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 1993

Total

Cleared

Denied

Aeros Instruments, Inc. has 4 FDA 510(k) cleared medical devices. Based in Northbrook, US.

Historical record: 4 cleared submissions from 1993 to 1995. Primary specialty: General & Plastic Surgery.

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

Aeros Instruments, Inc. 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 - Aeros Instruments, Inc.

5 devices

1-5 of 5