Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014831255

FEI Number

3014831255

Entity Name

LIQUIMEDLOCK

City/State/Country

Markham Ontario, CA

Establishment Address

3760 14th Avenue, Suite 203, Markham Ontario L3R3T7, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Liquimedlock (Owner Number: 10058354)

Owner / Operator Contact Address

3760 14th Avenue, Suite 203, Markham, CA-ON L3R3T7, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE ADAPTOR, HOLDER, SYRINGE CONTAINER, SPECIMEN, STERILE CONTAINER, LIQUID MEDICATION, GRADUATED

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2018-08-30
IQG	Adaptor, Holder, Syringe	Physical Medicine	Class 1	890.5050	2019-03-21
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2021-01-25
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2018-08-30

Official Correspondent

No official correspondent registered.

US Agent Details

Hector Matos Business: Retro Consultants, LLC Email: info@fdaregistrationassistance.com Phone: (928) 2758333

Related Public Records

Same Entity

Liquimedlock

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 3014831255. Last updated year: 2026. Please use registration number 3014831255 when referencing this establishment in official correspondence.