# Sterigenics U.S., LLC (contract sterilizer, Santa Teresa, NM): 17 new FDA device listings, incl. apron, leaded

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Sterigenics U.S., LLC |
| Owner / operator | Sotera Health LLC |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Santa Teresa, NM, US |
| New listings | 17 |
| Devices | Apron, Leaded; Catheter, Continuous Flush; Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter; Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation; Catheter, Intracardiac Mapping, High-Density Array; Table, Cystometric, Electric; Catheter, Electrode Recording, Or Probe, Electrode Recording; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation; Catheter, Ultrasound, Intravascular; Catheter, Percutaneous, Neurovasculature |
| Product codes | EAJ, KRA, OAD, OAE, MTD, MMZ, DRF, QZI, OBJ, QJP, DQY, IYO, BTR |
| Device classes | Class I, Class II, Class III |
| Medical specialties | Radiology, Cardiovascular, Gastroenterology, Urology, Anesthesiology |
| Brand names | Shiley TaperGuard Evac Oral Tracheal Tube, Murphy Eye |
| First new listing | 2026-06-25 |
| Latest new listing | 2026-09-01 |
| FDA registration number | 1721686 |
| Registration expires | 2026-12-31 |

## 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.