# Midwest Sterilization Corp. (contract sterilizer, Jackson, MO): 20 new FDA device listings, incl. stimulator, spinal-cord, implanted (pain relief)

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Midwest Sterilization Corp. |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Jackson, MO, US |
| New listings | 20 |
| Devices | Stimulator, Spinal-Cord, Implanted (Pain Relief); Aortic Valve, Prosthesis, Percutaneously Delivered; Catheter, Ultrasound, Intravascular; Electrode, Spinal Epidural; Catheter, Percutaneous; Prosthesis, Mitral Valve, Percutaneously Delivered; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation; Cover, Burr Hole; System, Appendage Closure, Left Atrial |
| Product codes | GZB, NPT, OBJ, LHG, DQY, NPU, QZI, GXR, NGV |
| Device classes | Class II, Class III |
| Medical specialties | Neurology, Cardiovascular |
| Brand names | Tripole™ Leads - 3214, 3219; Swift-Lock™ Anchor - 1192; Aortic valve, prosthesis, percutaneously delivered; Catheter, Ultrasound, Intravascular; Epiducer™ Lead Delivery System - 1771, 1772, 1773; Catheter, percutaneous; Prosthesis, mitral valve, percutaneously delivered; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation |
| First new listing | 2026-05-14 |
| Latest new listing | 2026-07-21 |
| FDA registration number | 1928237 |
| 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.