Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015219192

FEI Number

3015219192

Entity Name

SHENZHEN FITCONN TECHNOLOGY CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

7th, Floor No.116 xiangshan road, luotian community, songgang street, Baoan, Shenzhen Guangdong 518105, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Shenzhen Fitconn Technology Co., Ltd (Owner Number: 10059755)

Owner / Operator Contact Address

7th, Floor No.116 xiangshan road, luotian community, songgang street, Baoan, Shenzhen, CN-GD 518105, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CNB69028, CNB69029, CNB69029S, CNB69031, CNB69031S CNB69012, CNB69015, CNB69016, CNB69017, CNB69018, CNB69020, CNB69021, CNB69022, CNB69025, CNB69021S, CNB69025S, CNB69026 CDC100,CDC100B,CDC200,CDC200S,CDC300S,CDC500,CDC500S, CDC500B COMPRESSOR NEBULIZER, Models: CNB69006,CNB69007,CNB69008,CNB69009,CNB69010, CNB69011 Anti Decubitus Mattress models FU-AM001,FU-AM001L,FU-AM002,FU-AM003,FU-AM004,FU-AM005,FU-AM006 FU-AM006B, FU-AM006S, FU-AM006L, FU-AM006BL, FU-AM006SL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BTI	Compressor, Air, Portable	Anesthesiology	Class 2	868.6250	2019-08-02
FNM	Mattress, Air Flotation, Alternating Pressure	General Hospital	Class 2	880.5550	2019-02-20

Official Correspondent

Keven Peng

US Agent Details

Tiejun Chai Tiejun Chai Business: TJ Chai Investment LLC Email: Terry.Chai.Nj@Hotmail.Com Phone: (908) 6361278

Related Public Records

Same Entity

Shenzhen Fitconn Technology Co., Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K900686	Medical Industries America, Inc.	MAXI COMPRESSORS	1990-04-26

Similar Registrations

Registration Number	Establishment Name	Location
3003803075	EMG TECHNOLOGY CO., LTD.	Taichung City, TW
3008496560	NINGBO GREETMED MEDICAL INSTRUMENTS CO., LTD.	Ningbo Zhejiang, CN
3007238566	BEIJING AEONMED CO., LTD.	Sanhe Hebei, CN
3012336822	GUANGDONG JINME MEDICAL TECHNOLOGY CO., LTD.	Foshan Guangdong, CN
2515872	DeVilbiss Healthcare LLC.	SOMERSET, PA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015219192. Last updated year: 2026. Please use registration number 3015219192 when referencing this establishment in official correspondence.