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Sign in to claim this brandNovosource, Inc.
US
Last updated May 23, 2026
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Catalogue (901)
Page 2 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Novosource Total Hip System | 1125-1250 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-5436 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-5032 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1215-5228 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2043 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-1250 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1220-0060 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1345-2803 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3420-5004 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5002 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-0048 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3115-1203 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-5436 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3220-5011 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-4034 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-3031 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3220-5005 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2105 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1260-5232 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-1011 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-1032 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-4056 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1415-6228 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-6228 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-6240 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1210-0046 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1220-0054 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1125-0008 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1335-4000 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3054 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1000-1002 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1100-0750 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 2200-5436 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-1021 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-4545 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-1031 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2102 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1260-5236 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1450-0008 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1415-5436 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1300-3202 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3211-0011 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2046 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5032 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5037 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1410-4000 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5023 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1714-154-101 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-1015 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1007 | 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 |