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

Sterigenics U.S., LLC (Santa Teresa, New Mexico): 17 new FDA device listings, incl. apron, leaded. Its amount of 17 is top-decile (96th percentile of 2,570 records). Dated 64 days ago, it serves as a historical benchmark. Score 80/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 17 · 96th percentile of 2,570 DeviceEstablishmentPulse records · 17.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 1 related NM DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentSterigenics U.S., LLC
Owner / operatorSotera Health LLC
RoleContract sterilizer
Establishment typesSterilize Medical Device for Another Party (Contract Sterilizer)
LocationSanta Teresa, NM, US
New listings17
DevicesApron, 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 codesEAJ, KRA, OAD, OAE, MTD, MMZ, DRF, QZI, OBJ, QJP, DQY, IYO, BTR
Device classesClass I, Class II, Class III
Medical specialtiesRadiology, Cardiovascular, Gastroenterology, Urology, Anesthesiology
Brand namesShiley TaperGuard Evac Oral Tracheal Tube, Murphy Eye
First new listing2026-06-25
Latest new listing2026-09-01
FDA registration number1721686
Registration expires2026-12-31
amount percentile96th of 2,570 (median 1, 17.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-09-01
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Sterigenics U.S., LLC and 2 New Mexico peers

  • New Mexico DeviceEstablishmentPulse records like this one: 2
  • Sterigenics U.S., LLC's amount: 96th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every New Mexico peer: $400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Sterigenics U.S., LLC in Santa Teresa, New Mexico?

Sterigenics U.S., LLC (Santa Teresa, NM), a contract sterilizer, added 17 FDA device listings between 2026-06-25 and 2026-09-01.

How does Sterigenics U.S., LLC compare to other New Mexico DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 17 is 17.0x the median of 1 across 2,570 records. It is 64 days old; check the official source for later updates before acting. Its Score of 80/100 puts it among the stronger signals in this feed.

Sterigenics U.S., LLC vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Sterigenics U.S., LLCSanta Teresa, NM1796th2026-09-01
Isomedix Operations Inc.S Plainfield, NJ1696th2026-09-28
Isomedix Operations Inc.Sandy, UT1395th2026-10-15
Isomedix Operations, Inc.Minneapolis, MN1295th2026-10-14

Related records

DeviceEstablishmentPulse: Contract sterilizer DeviceEstablishmentPulse: U.S. establishment

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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.

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