ScreenDx is an AI-enabled medical device from Imvaria, Inc that the U.S. FDA cleared through 510(k) K241891 on January 10, 2025. Its lead review panel is Radiology and its primary product code is QWO (Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.).
See also FDA-cleared AI radiology devices in 2025, all FDA AI clearances in 2025, top radiology AI devices.
Key facts
| Submission number | K241891 |
|---|---|
| Pathway | 510(k) |
| Date of final decision | |
| Company (FDA list) | Imvaria, Inc |
| Lead review panel | Radiology |
| Primary product code | QWO — Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease. |
| Applicant (openFDA) | Imvaria, Inc. |
| Applicant location | Berkeley, CA, US |
| Device class | Class 2 |
| Regulation number | 21 CFR 892.2085 |
| Decision code | SESE |
| Submission type | Traditional |
Source: FDA AI-Enabled Medical Devices list and openFDA.
What this means
A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. ScreenDx went through this pathway (K241891).
openFDA lists it as a Class 2 device under 21 CFR 892.2085. Class II devices are moderate risk and are subject to general and special controls.
Product code QWO covers 4 devices on the FDA AI list. By decision date, this device is #3 of 4 under that code. Imvaria, Inc has 3 AI-enabled devices on the list, and the Radiology panel accounts for 1,230 in total.
Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.
Similar devices (product code QWO)
- Fibresolve (with PCCP)Imvaria, Inc. · Radiology
- IQ-UIPImbio, Inc. · Radiology
- FibresolveImvaria, Inc · Radiology