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Otto Bock Healthcare Products GmbH

FDA Regulatory Profile

Otto Bock Healthcare Products GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 22, 2026.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253256myosmart. (13E522); myosmart.cuff (757M20-2); connectgrip. (560X27-1); myosmart trial kit (642V64=T)April 22, 2026
K191179Myo PlusSeptember 4, 2019
K141812MYGAIT STIMULATION SYSTEMApril 2, 2015

FDA data resources