Medical Device Manufacturer · CA , Edmonton

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

2 submissions · 2 cleared · Since 2016

Recent clearances: Prelivia

Total

Cleared

Denied

Rehabtronics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Edmonton, CA.

Last cleared in 2021. Active since 2016. Primary specialty: Physical Medicine.

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

Rehabtronics, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Rehabtronics, Inc.

2 devices

1-2 of 2