Company · US
Medcad
FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2026. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 27, 2026 | K252064 | MedCAD® AccuStride System Medcad | PBF |
| Nov 4, 2025 | K251709 | MedCAD® AccuStride System Medcad | PBF |
| Mar 13, 2025 | K241811 | MedCAD® AccuStride System Medcad | PBF |
| Sep 26, 2023 | K230398 | MedCAD® AccuPlate® 3DTi Patient-Specific Plating System Medcad | JEY |
| Sep 20, 2023 | K223421 | MedCAD AccuPlan Orthopedics System Medcad | PBF |
| Mar 7, 2023 | K223024 | MedCAD AccuPlan System Medcad | DZJ |
| Aug 26, 2022 | K220357 | MedCAD AccuShape Titanium Patient-Specific Cranial Implant Medcad | GXN |
| Feb 12, 2021 | K193280 | MedCAD® AccuPlate® Patient-Specific Plate Medcad | JEY |
| Oct 29, 2020 | K192282 | MedCAD® AccuPlan® System Medcad | DZJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||