Prollenium Medical Technologies Inc.

FDA Device Registration & Listing · Richmond Hill Ontario, CA · Registration 3019585045

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
3019585045
FEI Number
3019585045
Entity Name
Prollenium Medical Technologies Inc.
City/State/Country
Richmond Hill Ontario, CA
Establishment Address
29 East Wilmot Street, Richmond Hill Ontario L4B1A3, CA
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Complaint File Establishment per 21 CFR 820.198,Foreign Private Label Distributor
Owner / Operator
Prollenium Medical Technologies Inc. (Owner Number: 10055618)
Owner / Operator Contact Address
138 Industrial Pkwy N., Aurora, CA-ON L4G4C3, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SoftFil® Precision SoftFil® EasyGuide

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2020-05-01

Official Correspondent

Denis Vezina

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Prollenium Medical Technologies Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004423487 PROLLENIUM MEDICAL TECHNOLOGIES INC. Aurora Ontario, CA

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019585045. Last updated year: 2026. Please use registration number 3019585045 when referencing this establishment in official correspondence.
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