# Midwest Sterilization Corp. (contract sterilizer, Laredo, TX): 13 new FDA device listings, incl. catheter, percutaneous

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Midwest Sterilization Corp. |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Laredo, TX, US |
| New listings | 13 |
| Devices | Catheter, Percutaneous; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation; Aortic Valve, Prosthesis, Percutaneously Delivered; System, Appendage Closure, Left Atrial; Prosthesis, Mitral Valve, Percutaneously Delivered; Catheter, Ultrasound, Intravascular |
| Product codes | DQY, QZI, NPT, NGV, NPU, OBJ |
| Device classes | Class II, Class III |
| Medical specialties | Cardiovascular |
| Brand names | Catheter, percutaneous; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation; Aortic valve, prosthesis, percutaneously delivered; System, appendage closure, left atrial; Prosthesis, mitral valve, percutaneously delivered; Catheter, Ultrasound, Intravascular |
| First new listing | 2026-07-21 |
| Latest new listing | 2026-07-21 |
| FDA registration number | 3005012805 |
| Registration expires | 2027-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- 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: 2026-10-28T20:51:27.468Z.
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.