Medical Device Manufacturer · DE , Magdeburg

Hasomed GmbH - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2007

Recent clearances: RehaStim 2, REHASTIM 2, ERIGOPRO (FES), REHASTIM 2, REHAMOVE 2

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hasomed GmbH Neurology ✕

4 devices

1-4 of 4

Cleared Feb 03, 2017

Neurology · 130d

Cleared May 28, 2014

REHASTIM 2, ERIGOPRO (FES)

Neurology · 299d

Cleared Oct 27, 2011

REHASTIM 2, REHAMOVE 2

Neurology · 28d

Cleared Dec 27, 2007

REHASTIM & REHAMOVE

Neurology · 41d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 16, 2026