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Sign in to claim this brandNovosource, Inc.
US
Last updated May 23, 2026
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Catalogue (901)
Page 4 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NovoKnee Total Knee System | 3301-2044 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1031 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-1036 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-4044 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1200-5836 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1012 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2044 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3055 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-6228 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1300-3601 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3201-0006 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-4014 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-1021 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-0750 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1445-3603 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3115-1205 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1450-0006 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1325-3603 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1300-4002 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-5228 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-2016 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1018 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1017 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-1105 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3220-5004 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3043 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2204 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-4003 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1415-4628 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1404-5032 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1210-0050 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5006 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3211-0016 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-4036 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1125-0009 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1435-2803 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-5828 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1435-2804 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1100-0002 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1125-0875 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1300-3602 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2042 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1210-0062 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-4035 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1020 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-4031 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5026 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-5228 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-3051 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1125-2250 | FDA UDI | Class II | Active |
Related Companies
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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 |