Otto Bock Healthcare Products GmbH

Otto Bock Healthcare Products GmbH holds 3 FDA 510(k) medical device clearances, first cleared 2015, most recent 2026.

Top product codes for Otto Bock Healthcare Products GmbH

GXY — Neurology2 devices
GZI — Neurology1 device

Recent clearances by Otto Bock Healthcare Products GmbH

K253256 — myosmart. (13E522); myosmart.cuff (757M20-2); connectgrip. (560X27-1); myosmart trial kit (642V64=T)Code GXY·2026-04-22
K191179 — Myo PlusCode GXY·2019-09-04
K141812 — MYGAIT STIMULATION SYSTEMCode GZI·2015-04-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.