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Sign in to claim this brandE-Med Innovations, Inc.
US
Last updated May 23, 2026
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- US
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Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Suction Easy | EMI610 CS | FDA UDI | Class I | Active |
| Suction Easy | EMI610 | FDA UDI | Class I | Active |
| Seaduc | EMI700 | FDA UDI | Class I | Active |
| Respire Disposable Pulmonary Resuscitator | K913474 | FDA 510(k) | Class II | Active |
| Anesthesia/Respiratory Face Mask, Various Sizes | K905288 | FDA 510(k) | Class I | Active |
| Disposable Heat & Mositure Exchanger & Filter/Hme | K944194 | FDA 510(k) | Class I | Active |
| Stickit | K935407 | FDA 510(k) | Class II | Active |
| E-Steth Electronic Stethoscope | K011898 | FDA 510(k) | 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 |
|---|---|---|---|---|
| Apr 3, 2006 | Z-0056-2007 | — | terminated | The firm failed to include User Instructions with the Stic Kit Needle Containment Device, Model EMI 82691, which they shipped to distributor/customers. |