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Sign in to claim this brandNovosource, Inc.
US
Last updated May 23, 2026
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Catalogue (901)
Page 3 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NovoKnee Total Knee System | 3311-4013 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-0028 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2033 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1058 | FDA UDI | Class I | Active |
| Novosource Total Hip System | 1215-5432 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-1013 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1404-5232 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-1500 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-0048 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2106 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1280-5436 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-4024 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5021 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-0068 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-4026 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1260-4628 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2104 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 2200-6640 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1100-0875 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3220-5000 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-4045 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-1046 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 2200-5232 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3021 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-0058 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-2043 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3051 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3201-0002 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1445-2803 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-6240 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-5432 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2023 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3115-1106 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1051 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1415-6232 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1052 | FDA UDI | Class I | Active |
| Novosource Total Hip System | 1210-0048 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-0045 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-2046 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-5836 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1125-1000 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1445-3205 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1125-1500 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1404-5028 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3111-1105 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-4015 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5074 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-4046 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-2052 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-1775 | FDA UDI | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 19, 2024 | Z-0483-2025 | — | open, classified | Mislabeled: Packaged in a box labeled as 32 long but containing a 28 long head by physical marking, may result in joint instability if implanted |