Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010367874

FEI Number

3010367874

Entity Name

TRICORBRAUN HONGKONG CORPORATION LIMITED

City/State/Country

Hongkong, HK

Establishment Address

Room 2202, 22/F., 168 Sai Yeung Choi Street,, Mongkok, Kowloon, Hong Kong, Hongkong 999077, HK

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

TRICORBRAUN HONGKONG CORPORATION LIMITED (Owner Number: 10043568)

Owner / Operator Contact Address

RM109, 11/F. Hip Sang Building,, 107-115 Hennessy Rd, Wanchai, Hongkong, HK-NOTA 999077, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2023-02-26
HDL	Retractor, Vaginal	Obstetrics/Gynecology	Class 1	884.4520	2023-02-26
KYX	Dispenser, Liquid Medication	General Hospital	Class 1	880.6430	2013-02-28

Official Correspondent

Hector Liang

US Agent Details

Karen Schnabel Business: TricorBraun Inc. Email: kschnabel@tricorbraun.com Phone: (562) 4836609

Related Public Records

Same Entity

TRICORBRAUN HONGKONG CORPORATION 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 3010367874. Last updated year: 2026. Please use registration number 3010367874 when referencing this establishment in official correspondence.