Sterisil

FDA Device Registration & Listing · Colorado Spgs, CO, US · Registration 3005844469

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005844469
FEI Number
3005844469
Entity Name
Sterisil
City/State/Country
Colorado Spgs, CO, US
Establishment Address
4220 Mark Dabling Blvd, Colorado Spgs, CO 80907, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Solmetex (Sterisil) (Owner Number: 9090239)
Owner / Operator Contact Address
4220 Mark Dabling Blvd, Colorado Springs, CO 80907, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Sterisil® Dental Water Microbiological – Inline Cartridge Sterisil® Dental Water Microbiological Cartridge - Stage 5 Sterisil® Dental Water Microbiological – Valved Cartridge Sterisil® Straw

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QYJ Dental Waterline Treatment Cartridge Dental Class 1 872.6640 2024-03-01

Official Correspondent

Curtis Conley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Solmetex (Sterisil)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005844469. Last updated year: 2026. Please use registration number 3005844469 when referencing this establishment in official correspondence.
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