Steris Corporation (repackager or relabeler, Breckenridge Hills, MO): 1 new FDA device listing, incl. interim reprocessing cleaning and intermediate-level disinfection wipe
Steris Corporation (Breckenridge Hills, Missouri): 1 new FDA device listing, incl. interim reprocessing cleaning and intermediate-level disinfection wipe. Its amount of 1 is above the median of 2 (50th percentile). Dated 153 days ago, it serves as a historical benchmark. Score 50/100. As of 2026-11-04, 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: 1 · 50th percentile of 2,709 DeviceEstablishmentPulse records · 0.5x the median
Free preview: all 15 published fields of this record are shown below. Locked: 13 related MO DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Steris Corporation |
| Owner / operator | STERIS Corporation |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Breckenridge Hills, MO, US |
| New listings | 1 |
| Devices | Interim Reprocessing Cleaning And Intermediate-Level Disinfection Wipe |
| Product codes | SHM |
| Device classes | Class II |
| Medical specialties | General Hospital |
| Brand names | Prolystica Pass-Thru Disinfectant Wipes (1C061D) (SL-CFE,SD, SLDC-RR) |
| First new listing | 2026-06-05 |
| Latest new listing | 2026-06-05 |
| FDA registration number | 1933443 |
| Registration expires | 2027-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
| Peer records CSV (14 MO records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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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: 2026-06-05
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (MO first): Midwest Sterilization Corp. (contract sterilizer, Jackson, M · Surgical Instrument Manufacturers, LLC (contract manufacture · Biomerieux, Inc. (manufacturer, Hazelwood, MO) · Biomerieux, Inc. (manufacturer, Hazelwood, MO) · Steris Corporation (manufacturer, Saint Louis, MO) · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Steris Corporation and 14 Missouri peers
- Missouri DeviceEstablishmentPulse records like this one: 14
- Steris Corporation's amount: 50th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Missouri peer: $2,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
50 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Steris Corporation in Breckenridge Hills, Missouri?
Steris Corporation (Breckenridge Hills, MO), a repackager or relabeler, added 1 FDA device listing on 2026-06-05.
How does Steris Corporation compare to other Missouri DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 153 days old; check the official source for later updates before acting.
Steris Corporation vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Steris Corporation | Breckenridge Hills, MO | 1 | 50th | 2026-06-05 |
| Gurin Products LLC | Tustin, CA | 3 | 77th | 2026-10-22 |
| Tpc Advanced Technology, Inc. | City Industry, CA | 4 | 83rd | 2026-09-28 |
| Uih Technologies, LLC | Houston, TX | 8 | 90th | 2026-10-21 |
Related records
DeviceEstablishmentPulse: Repackager or relabeler DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Missouri
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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.