ORCHID Orthopedic Solutions, Ltd.
ORCHID Orthopedic Solutions, Ltd. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jun 18, 2025 · VAI
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 5 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jun 18, 2025 | Holt, MI | Devices | Voluntary Action Indicated (VAI) | 3005852519 |
| May 11, 2017 | Sheffield, United Kingdom | Devices | No Action Indicated (NAI) | 3010089671 |
| Mar 20, 2014 | Sheffield, United Kingdom | Devices | No Action Indicated (NAI) | 3010089671 |
| Jan 27, 2011 | Sheffield, United Kingdom | Devices | Voluntary Action Indicated (VAI) | 3010089671 |
| Oct 20, 2008 | Sheffield, United Kingdom | Devices | No Action Indicated (NAI) | 3010089671 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3005852519 | Holt, MI | 1 | Jun 18, 2025 |
| FEI 3010089671 | Sheffield, United Kingdom | 4 | May 11, 2017 |