Cymedica Orthopedics, Inc.
Cymedica Orthopedics, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Mar 22, 2023
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 5 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K230533 | Motive Electrode | Mar 22, 2023 |
| K220738 | Motive Knee Wrap | May 12, 2022 |
| K210604 | Intellihab System | Jun 3, 2021 |
| K163067 | CyMedica e-vive System; CY-1000 | Dec 1, 2016 |
| K150413 | QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator | Apr 2, 2015 |