# Rapid Medical Inc. (other, Southlake, TX): 4 new FDA device listings, incl. guide, wire, catheter, neurovasculature

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Rapid Medical Inc. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Southlake, TX, US |
| New listings | 4 |
| Devices | Guide, Wire, Catheter, Neurovasculature; Wire, Guide, Catheter; Catheter, Thrombus Retriever |
| Product codes | MOF, DQX, NRY |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | Drivewire 35 Guidewire; Hyperdrive 35 Guidewire; Tigertriever 13 Ultra (Micro) Revascularization Device |
| First new listing | 2026-07-19 |
| Latest new listing | 2026-09-20 |
| FDA registration number | 3015531723 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- 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: 2026-11-04T21:52:36.524Z.
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.
