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Sign in to claim this brandCrospon, Ltd.
US
Last updated May 23, 2026
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Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| EndoFLIP | EF-322 | FDA UDI | Class II | Active |
| Esoflip Balloon Dilation Catheter | K132337 | FDA 510(k) | Class II | Active |
| EndoFLIP | K160725 | FDA 510(k) | Class II | Active |
| Endoflip Gastric Tube | K110529 | FDA 510(k) | Class II | Active |
| Endoflip Catheter | K130906 | FDA 510(k) | Class II | Active |
| EsoFLIP® ES-310 Balloon Catheter | K172128 | FDA 510(k) | Class II | Active |
| EndoFLIP® System with FLIP Topography module | K170833 | FDA 510(k) | Class II | Active |
| Barostat Software Option | K120997 | FDA 510(k) | Class II | Active |
| EndoFLIP System | K183072 | FDA 510(k) | Class II | Active |
| Esoflip Es | K142000 | FDA 510(k) | Class II | Active |
| Endoflip | K092850 | FDA 510(k) | Class II | Active |
| Endoflip Ecd | K110531 | FDA 510(k) | Class II | Active |
| Endo Flip | K102214 | FDA 510(k) | Class II | Active |
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