Otto Bock Healthcare Products GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253256 | myosmart. (13E522); myosmart.cuff (757M20-2); connectgrip. (560X27-1); myosmart trial kit (642V64=T) | April 22, 2026 |
| K191179 | Myo Plus | September 4, 2019 |
| K141812 | MYGAIT STIMULATION SYSTEM | April 2, 2015 |