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Sign in to claim this brandVORTRAN MEDICAL TECHNOLOGY 1, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 21 Goldenland Court, SACRAMENTO, CA, 95834
- Website
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000307109
- DUNS Number
- —
Catalogue (55)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vmt Hand Held Nebulizer | K841894 | FDA 510(k) | Class I | Active |
| Autoneb Breath Actuated Controller And Accessory Kit | K935693 | FDA 510(k) | Class II | Active |
| Vmt Gentle-Haler | K842988 | FDA 510(k) | Class I | Active |
| Var-Plus (vortran Automatic Resuscitator), Model Pcm | K041473 | FDA 510(k) | Class II | Active |
| Var Monitor | K073261 | FDA 510(k) | Class II | Active |
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FDA Recalls (2)
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 20, 2017 | Z-2092-2017 | — | terminated | Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the wrong thread direction. |
| Apr 20, 2017 | Z-2091-2017 | — | terminated | Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the wrong thread direction. |