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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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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000307109
- DUNS Number
- —
Catalogue (55)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VAR (VORTRAN Automatic Resuscitator) with Extension | PTE-5002 | FDA UDI | Class II | Active |
| VAR (VORTRAN Automatic Resuscitator) with Manometer | PCM-5011 | FDA UDI | Class II | Active |
| VCI (VORTRAN Cuff Inflator) | 2450 | FDA UDI | Class II | Active |
| VORTRAN-IPPB with Manomter | IPM-4022 | FDA UDI | Class II | Active |
| VORTRAN PercussiveNEB 2.0 | 8030 | FDA UDI | Class II | Active |
| VORTRAN GO2VENT® with Peep Valve | 6123 | FDA UDI | Class II | Active |
| VAR-Monitor | VM-3500 | FDA UDI | Class II | Active |
| VORTRAN GO2VENT with PEEP Valve | 6200 | FDA UDI | Class II | Active |
| VORTRAN® APM-Plus | 3960 | FDA UDI | Class II | Active |
| VAR (VORTRAN Automatic Resuscitator) with Manometer | PTM-5001 | FDA UDI | Class II | Active |
| VAR Surgical Center Kit | PCK-5050 | FDA UDI | N/A | Active |
| Vortran Manometer | 6030 | FDA UDI | Class II | Active |
| Vortran Go2vent | 6123-16 | FDA UDI | Class II | Active |
| VAR (VORTRAN Automatic Resuscitator) | PC-5010 | FDA UDI | Class II | Active |
| Vortran Go2vent | 6600 | FDA UDI | Class II | Active |
| E-Surge Kit | ES-4070 | FDA UDI | N/A | Active |
| VORTRAN-IPPB with Water Trap | IPW-4021 | FDA UDI | Class II | Active |
| Vortran Manometer | 6031 | FDA UDI | Class II | Active |
| VORTRAN PercussiveNEB | PNB-4030 | FDA UDI | Class II | Active |
| VAR (VORTRAN Automatic Resuscitator) with Extension | PCE-5012 | FDA UDI | Class II | Active |
| Vortran Go2vent | 6001 | FDA UDI | Class II | Active |
| Vortran Go2vent | 6123 | FDA UDI | Class II | Active |
| VORTRAN Medical Air Compressor | 8100 | FDA UDI | Class II | Active |
| VORTRAN PercussiveNEB 2.0 w/ Top Nebulizer Port | 8040 | FDA UDI | Class II | Active |
| VAR (VORTRAN Automatic Resuscitator) | PT-5000 | FDA UDI | Class II | Active |
| VORTRAN Airway Pressure Monitor | APM-3900 | FDA UDI | Class II | Active |
| Vortran-Ippb | IP-4020 | FDA UDI | Class II | Active |
| Aerosol Charging Adaptor (for Use W/Minineb Only) | K924667 | FDA 510(k) | Class II | Active |
| Respirtechpro | K973975 | FDA 510(k) | Class II | Active |
| Autoneb Accessory Cross (aac) | K944643 | FDA 510(k) | Class II | Active |
| Heart Nebulizer #100609 | K963910 | FDA 510(k) | Class II | Active |
| Vortran Airway Pressure Monitor (vapm)-Adult, Vortran Airway Pressure Monitor (vapm)- Pediatric | K103639 | FDA 510(k) | Class II | Active |
| (heart) Nebulizer | K896696 | FDA 510(k) | Class II | Active |
| Soft-Mist(tm) | K924649 | FDA 510(k) | Class II | Active |
| Vortran Intermittent Signal Activated Nebulizer | K911759 | FDA 510(k) | Class II | Active |
| VORTRAN GO2VENT with PEEP Valve | K202219 | FDA 510(k) | Class II | Active |
| VORTRAN Cuff Inflator (VCI) | K173914 | FDA 510(k) | Class II | Active |
| Percussiveneb, Model Pn-2001 | K003684 | FDA 510(k) | Class II | Active |
| Venti-Gentle-Haler(tm) | K933915 | FDA 510(k) | Class II | Active |
| Uniheart | K943600 | FDA 510(k) | Class II | Active |
| Vortran Go2vent | K162968 | FDA 510(k) | Class II | Active |
| Intermittent Signal Actuated Nebulizer (visan) | K873477 | FDA 510(k) | Class I | Active |
| Heart Nebulizer | K923596 | FDA 510(k) | Class II | Active |
| Minineb | K920443 | FDA 510(k) | Class II | Active |
| Percussivetech Hf, Model 2001 | K981726 | FDA 510(k) | Class II | Active |
| VORTRAN Manometer | K153733 | FDA 510(k) | Class II | Active |
| Respirtech Pro-O2c, Model 2200 And Respirtech Pro, Model 2000 | K001430 | FDA 510(k) | Class II | Active |
| Heart Nubulizer | K920332 | FDA 510(k) | Class II | Active |
| Piper Ippb Model 2055 | K982016 | FDA 510(k) | Class II | Active |
| VORTRAN APM-Plus | K182292 | 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. |