Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030379986

FEI Number

3030379986

Entity Name

CERIE INTERNATIONAL LIMITED

City/State/Country

Hong Kong, HK

Establishment Address

30/F, Asia Trade Centre, 79 Lei Muk Road,, Kwai Chung, N.T., Hong Kong, Hong Kong 999077, HK

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Cerie International Limited (Owner Number: 10088565)

Owner / Operator Contact Address

30/F, Asia Trade Centre, 79 Lei Muk Road,, Kwai Chung, N.T., Hong Kong, Hong Kong, HK-NOTA 999077, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Knix

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUQ	Pad, Menstrual, Reusable	Obstetrics/Gynecology	Class 1	884.5435	2024-05-29

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

Cerie International Limited

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 3030379986. Last updated year: 2026. Please use registration number 3030379986 when referencing this establishment in official correspondence.