Data / Medical devices / United States / Corvent Medical Inc.
Corvent Medical Inc.: FDA-registered device maker in Fargo, ND, United States, 2 510(k) clearances
Corvent Medical Inc. is registered with the FDA (registration 3033571078) in Fargo, ND, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033571078
- Address
- 4837 Amber Valley Parkway S Suite #2, Fargo, ND, United States, 58104
- Owner or operator
- CorVent Medical Inc. (10092028)
- Roles
- Manufacturer
- First device listed
- November 26, 2024
- Registered through
- 2026
- Brand names listed
- CorVision, RESPOND Ventilator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory To Continuous Ventilator (Respirator) | MOD | 2 | Manufacturer | accessdata.fda.gov |
| Ventilator, Continuous, Facility Use | CBK | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 12, 2026 | K260051 | CorVision® (91-205-Z0014) | MOD | Substantially Equivalent | CorVent® Medical, Inc. | accessdata.fda.gov |
| November 13, 2024 | K241135 | RESPOND(R) Ventilator | CBK | Substantially Equivalent | Corvent Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Ventilator, Continuous, Facility Use
- All makers of Accessory To Continuous Ventilator (Respirator)
Updated May 12, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.