Medical Device Manufacturer · US , Memphis , TN

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

6 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Innervision, Inc. has 6 FDA 510(k) cleared medical devices. Based in Memphis, US.

Historical record: 6 cleared submissions from 1994 to 1999. Primary specialty: General & Plastic Surgery.

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

Innervision, 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 - Innervision, Inc.

6 devices

1-6 of 6