Medical Device Manufacturer · US , Crofton , MD

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

2 submissions · 2 cleared · Since 2012

Total

Cleared

Denied

Nanovibronix, Inc. has 2 FDA 510(k) cleared medical devices. Based in Crofton, US.

Last cleared in 2022. Active since 2012. Primary specialty: General & Plastic Surgery.

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

Nanovibronix, 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 - Nanovibronix, Inc.

2 devices

1-2 of 2