# Medtronic CryoCath LP (manufacturer, Pointe-Claire Quebec, CA): 1 new FDA device listing, incl. cardiac ablation percutaneous catheter

**Score:** 60/100

| Field | Value |
|---|---|
| Establishment | Medtronic CryoCath LP |
| Owner / operator | Medtronic, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Pointe-Claire Quebec, CA |
| New listings | 1 |
| Devices | Cardiac Ablation Percutaneous Catheter |
| Product codes | LPB |
| Device classes | Class III |
| Brand names | Freezor Xtra; Freezor |
| First new listing | 2026-05-26 |
| Latest new listing | 2026-05-26 |
| FDA registration number | 3002648230 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.

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.