Bo Cheng Technology Co., Ltd., Dongguan City

FDA Device Registration & Listing · Dongguan City Guangdong, CN · Registration 3018270012

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
3018270012
FEI Number
3018270012
Entity Name
Bo Cheng Technology Co., Ltd., Dongguan City
City/State/Country
Dongguan City Guangdong, CN
Establishment Address
Yantian Jingbo Industrial Park E, 5th Floor, Fenggang Town,, Dongguan City Guangdong 523000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Inno Team Industrial Company Limited (Owner Number: 10080451)
Owner / Operator Contact Address
Room 6, 13 Floor, Mai Wo Industrial Building,, 90-98 Kwai Cheong Road, Kwai Chung, New Territories, Hong Kong, HK-NOTA 852, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Laryngeal Oral Airway

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2021-02-07

Official Correspondent

Chan Yau Chan

US Agent Details

Sangita Lakhia Business: Sinus & Snoring Specialists Email: slakhias3@icloud.com Phone: (512) 5961424

Related Public Records

Same Entity

Inno Team Industrial Company Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2014 King Systems Corp. 1
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018270012. Last updated year: 2026. Please use registration number 3018270012 when referencing this establishment in official correspondence.
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