NIXIT LIMITED

FDA Device Registration & Listing · Toronto Ontario, CA · Registration 3014926189

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
3014926189
FEI Number
3014926189
Entity Name
NIXIT LIMITED
City/State/Country
Toronto Ontario, CA
Establishment Address
18 King Street East, Suite 1400, Toronto Ontario M5C 1C4, CA
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Nixit Limited (Owner Number: 10058811)
Owner / Operator Contact Address
18 King Street East, Suite 1400, Toronto, CA-ON M5C 1C4, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Nixit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2018-10-30

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Nixit Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014926189. Last updated year: 2026. Please use registration number 3014926189 when referencing this establishment in official correspondence.
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