Medical Device Manufacturer · US , Bensenville , IL

Sensory Aids Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1986

Total

Cleared

Denied

Sensory Aids Corp. has 4 FDA 510(k) cleared medical devices. Based in Bensenville, US.

Historical record: 4 cleared submissions from 1986 to 1987. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Sensory Aids Corp. Filter by specialty or product code using the sidebar.

Sensory Aids Corp. 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 - Sensory Aids Corp.

4 devices

1-4 of 4