Splint, Intranasal Septal
FDA product code LYA · Class 1 · 20 devices · 40 reports · 12 devices named in recalls
- Nasopore 5400030008Stryker Corporation · SPLINT, INTRANASAL SEPTAL2 recalls1 report
- Nasopore 5400010008Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall4 reports
- Nasopore 5400020108Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall3 reports
- Hemopore 5400020208Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall3 reports
- ORCA Foam StandardOrca Products, LLC · Splint, Intranasal Septal1 recall0 reports
- Nasopore 5400010004Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Nasopore 5400020004Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Nasopore 5400020008Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Nasopore 5400030004Stryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Nasopore 5400212004sStryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Nasopore 5400222004SStryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Hemopore 5400222208SStryker Corporation · SPLINT, INTRANASAL SEPTAL1 recall0 reports
- Rapid Rhino RR1000Smith & Nephew, Inc. · SPLINT, INTRANASAL SEPTAL12 reports
- ChitoZolve CNS155Gyrus ACMI, LLC · Splint, Intranasal Septal8 reports
- Rapid Rhino RR 800Smith & Nephew, Inc. · SPLINT, INTRANASAL SEPTAL3 reports
- Sinu-foam RR 650Smith & Nephew, Inc. · SPLINT, INTRANASAL SEPTAL2 reports
- Sinu-Knit RR 600Smith & Nephew, Inc. · SPLINT, INTRANASAL SEPTAL1 report
- Gyrus ACMI 890919Gyrus ACMI, LLC · SPLINT, INTRANASAL SEPTAL1 report
- NA 5450825000Stryker Medtech K.K. · SPLINT, INTRANASAL SEPTAL1 report
- Doyle II ™ 1524050Medtronic Xomed, Inc. · SPLINT, INTRANASAL SEPTAL1 report