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Sign in to claim this brandTherox, Inc.
US
Last updated May 30, 2026
What Therox, Inc. makes
Therox, Inc. manufactures devices for supersaturated oxygen therapy, including catheters, cartridges, and complete system components. Their portfolio includes infusion guidewires, catheters like the THEROX INFUSION CATHETER (Model INCA-1), and systems designed to deliver oxygen therapy via supersaturated solutions. Examples include the SSO2 Catheter, DownStream Cartridge, and the DownStream System.
The company’s products are regulated under FDA pathways, with devices classified as Class II and Class III. They appear in the FDA’s 510(k) and UDI registries. Therox, Inc. is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- therox.com
- —
- —
- [email protected]
- Phone
- 949-757-1999
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 835420894
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SSO2 Catheter | SSO2 - 4.5 | FDA UDI | Class III | Active |
| DownStream Cartridge | DSC-2 | FDA UDI | Class III | Active |
| SSO2 Catheter | SSO2 - 5.0 | FDA UDI | Class III | Active |
| DownStream System | DS-1 (Refurbished) | FDA UDI | Class III | Active |
| DownStream System | DS-1 | FDA UDI | Class III | Active |
| SSO2 Catheter | SSO2 - 3.5 | FDA UDI | Class III | Active |
| SSO2 Catheter | SSO2 - 4.0 | FDA UDI | Class III | Active |
| Therox Infusion Guidewires | K971719 | FDA 510(k) | Class II | Active |
| Therox Infusion Catheter, Model Inca-1 | K052637 | FDA 510(k) | Class II | Active |
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