Data / Medical devices / United States / Argus Cognitive, Inc.
Argus Cognitive, Inc.: FDA-registered device maker in Hanover, NH, United States, 2 510(k) clearances
Argus Cognitive, Inc. is registered with the FDA (registration 3036502204) in Hanover, NH, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 9, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036502204
- Address
- 35 S Main St, Hanover, NH, United States, 03755
- Owner or operator
- Argus Cognitive, Inc. (10092807)
- Roles
- Manufacturer
- First device listed
- February 20, 2025
- Registered through
- 2026
- Brand names listed
- ReVISION, ReVISION 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automated Radiological Image Processing Software | QIH | 2 | Manufacturer | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| September 9, 2026 | K251417 | ReVISION 2 | QIH | Substantially Equivalent | Argus Cognitive, Inc. | accessdata.fda.gov |
| July 24, 2023 | K223322 | Argus Cognitive ReVISION Software | LLZ | Substantially Equivalent | Argus Cognitive, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Image Processing, Radiological
- All makers of Automated Radiological Image Processing Software
Updated September 9, 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.