Data / Medical devices / United States / NEUROCAREAI INC (DBA SaveLife.AI)
NEUROCAREAI INC (DBA SaveLife.AI): FDA-registered device maker in Prosper, TX, United States, 2 510(k) clearances
NEUROCAREAI INC (DBA SaveLife.AI) is registered with the FDA (registration 3034656245) in Prosper, TX, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 4, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3034656245
- Address
- 1740 Lonesome Dove Dr, Prosper, TX, United States, 75078
- Owner or operator
- NEUROCAREAI INC (10092202)
- Roles
- Manufacturer
- First device listed
- December 12, 2024
- Registered through
- 2026
- Brand names listed
- MammoSightAI
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Radiological Computer-Assisted Prioritization Software For Lesions | QFM | 2 | Manufacturer | accessdata.fda.gov |
| Radiological Computer-Assisted Triage And Notification Software | QAS | 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 4, 2026 | K252954 | MammoSightAI | QFM | Substantially Equivalent | Neurocareai, Inc. (Dba Savelife.Ai) | accessdata.fda.gov |
| November 7, 2024 | K241719 | NeuroICH | QAS | Substantially Equivalent | Neurocareai, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Radiological Computer-Assisted Triage And Notification Software
- All makers of Radiological Computer-Assisted Prioritization Software For Lesions
Updated May 4, 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.