Light, Surgical, Fiberoptic
FDA product code FST · Class 2 · 22 devices · 121 reports · 0 devices named in recalls
- NA 242386Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC49 reports
- Arthrex® AR-3240-5027Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC30 reports
- Integra® 001388LX9Integra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC7 reports
- N/A FC1SPStryker Corporation · Light, Surgical, Fiberoptic5 reports
- UltraLite® AX2100BIFIntegra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC4 reports
- Arthrex® AR-3240-5040Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC3 reports
- NA 242387Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC3 reports
- MaXcess 1025461Nuvasive, Inc. · LIGHT, SURGICAL, FIBEROPTIC2 reports
- MaXcess 3200220Nuvasive, Inc. · LIGHT, SURGICAL, FIBEROPTIC2 reports
- Arthrex® AR-3240-3530Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC2 reports
- LITe DECOMPRESSION 48089999Stryker Corporation · LIGHT, SURGICAL, FIBEROPTIC2 reports
- NA 242388Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC2 reports
- NuVasive 4221110Nuvasive, Inc. · LIGHT, SURGICAL, FIBEROPTIC1 report
- N/A FC1BStryker Corporation · Light, Surgical, Fiberoptic1 report
- MI Product Line 061524Medical Illumination International Inc. · Light, Surgical, Fiberoptic1 report
- MI Product Line 061525Medical Illumination International Inc. · Light, Surgical, Fiberoptic1 report
- MaXcess 1025462Nuvasive, Inc. · LIGHT, SURGICAL, FIBEROPTIC1 report
- Arthrex® AR-3240-3527Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC1 report
- Arthrex® AR-3240-5028Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC1 report
- UltraLite® AX1375BIFIntegra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC1 report
- Snowden-Pencer 88-9760Steris Corporation · LIGHT, SURGICAL, FIBEROPTIC1 report
- NA 242391Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC1 report