# Caranx, Inc. (other, Claymont, DE): 2 new FDA device listings, incl. interventional fluoroscopic x-ray system

**Score:** 50/100

| Field | Value |
|---|---|
| Establishment | Caranx, Inc. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Claymont, DE, US |
| New listings | 2 |
| Devices | Interventional Fluoroscopic X-Ray System; Automated Radiological Image Processing Software |
| Product codes | OWB, QIH |
| Device classes | Class II |
| Medical specialties | Radiology |
| Brand names | TAVIPILOT Software |
| First new listing | 2026-07-15 |
| Latest new listing | 2026-07-15 |
| FDA registration number | 3047842058 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.