Qlrad Inc

FDA Device Registration & Listing · Miami, FL, US · Registration 3010472281

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
3010472281
FEI Number
3010472281
Entity Name
Qlrad Inc
City/State/Country
Miami, FL, US
Establishment Address
80 SW 8th street, suite 2000, Miami, FL 33130, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
QLRAD International Ltd. (Owner Number: 10025073)
Owner / Operator Contact Address
Damsluisweg 6, Almere, NL-FL 1332 EC, NL
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Inframammary Fold Breast Wedge

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPY Shield, Protective, Personnel Radiology Class 1 892.6500 2023-10-12

Official Correspondent

Arjen Winkel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

QLRAD International Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3006948745 QLRAD Almere Flevoland, NL

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010472281. Last updated year: 2026. Please use registration number 3010472281 when referencing this establishment in official correspondence.
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