Data / Medical devices / United States / Neuros Medical Inc.
Neuros Medical Inc.: FDA-registered device maker in Arden Hills, MN, United States, 1 PMA approval
Neuros Medical Inc. is registered with the FDA (registration 3026283936) in Arden Hills, MN, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated August 26, 2024. Registered through 2026. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3026283936
- Address
- 1212 Red Fox Rd, Arden Hills, MN, United States, 55112
- Owner or operator
- Neuros Medical Inc. (10091346)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- August 31, 2024
- Registered through
- 2026
- Brand names listed
- Altius BC, Altius Cuff Large, Altius Cuff Medium, Altius Cuff Small, Altius IPG, Altius IPG Accessory Kit, Altius PAPC, Altius PTC and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve Terminus, Totally Implanted For Chronic Intractable Post-Amputation Pain Of The Lower Limb | SAZ | 3 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| August 26, 2024 | P230020 | Altius® Direct Electrical Nerve Stimulation System | SAZ | 8 | October 16, 2026 | accessdata.fda.gov |
Updated October 16, 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.