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Sign in to claim this brandNovosource, Inc.
US
Last updated May 23, 2026
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Catalogue (901)
Page 5 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Novosource Total Hip System | 1300-4001 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-3053 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-2054 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1220-0056 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-0055 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3036 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-6232 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3320-5000 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1260-6236 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-4002 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-2031 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3013 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-6636 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3220-5023 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5028 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1425-0722 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1204-5028 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5005 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1325-4003 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5018 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-5236 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-0060 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1100-1125 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1400-6236 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-1013 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-0046 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1300-4004 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3115-1202 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3115-1201 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-5028 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1300-4003 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1345-3601 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-1060 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1125-0002 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-3056 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3111-1103 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3120-5011 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1450-0004 | FDA UDI | Class II | Active |
| NovoHip Total Hip System | 1500-0061 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3211-0005 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3301-3053 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3211-0002 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3111-1101 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3201-0001 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1325-3604 | FDA UDI | Class II | Active |
| Novosource Total Hip System | 1200-5432 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2201 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3111-1205 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3101-2203 | FDA UDI | Class II | Active |
| NovoKnee Total Knee System | 3311-3033 | 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 |