Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007307590

FEI Number

3007307590

Entity Name

Shenzhen Contin Medical Device Co., Ltd.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Unit B&C,6/F, Building 2,Zhongcheng Biomedical Industrial Park, No.21 Linhui Road, Kengzi Street, Pingshan District, Shenzhen Guangdong 518118, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Shenzhen Contin Medical Device Co., Ltd. (Owner Number: 10027256)

Owner / Operator Contact Address

Unit B&C,6/F, Building 2,Zhongcheng Biomedical Industrial Park, No.21 Linhui Road, Kengzi Street, Pingshan District, Shenzhen, CN-GD 518118, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pressure Pad Alarm Bed Patient Monitor Monitor, Bed patient Under the Mattress Pad Under the Seat Alarm Systems Magnet Alarm Floor Mat Seat Belt Toilet Sensor Pad Nurse Call Button Air Push Call Button Fall Prevention Alarm/Sensor Combination Attached Or Unattached

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMI	Monitor, Bed Patient	General Hospital	Class 1	880.2400	2008-10-18
PJO	Fall Prevention Alarm/Sensor Combination Attached Or Unattached	General Hospital	Class 1	880.2400	2024-11-26

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Shenzhen Contin Medical Device Co., Ltd.

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 3007307590. Last updated year: 2026. Please use registration number 3007307590 when referencing this establishment in official correspondence.