Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016710934

FEI Number

3016710934

Entity Name

MEDICO TECHNOLOGY CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Room 201, 301 and 401 Building A No.10, Bao long 5th Road, Tongle Community, Baolong Street, Longgang District, Shenzhen Guangdong 518172, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MEDICO TECHNOLOGY CO., LTD (Owner Number: 10063982)

Owner / Operator Contact Address

Room 201, 301 and 401 Building A No.10, Bao long 5th Road, Tongle Community, Baolong Street, Longgang District, Shenzhen, CN-GD 518172, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DNA Sampling Kit,Virus Sampling Kit,Influenza Sampling Kit,Virus Transport Medium Specimen Collection Swab Phosphate Buffered Saline(PBS) Phosphate Buffer Saline Virus Transport Medium Sample Transportation Buffer Disposable virus sampling kit Amies Buffer Amies Buffer Phosphate Buffer Saline Virus Transport Medium Sample Transportation Buffer Phosphate Buffered Saline(PBS) Disposable virus sampling kit Provox Swab Small,Provox Swab Medium,Provox Swab Large,Provox Swab XtraLarge Sample Transportation Buffer Virus Transport Medium Phosphate Buffer Saline Disposable virus sampling kit Phosphate Buffered Saline(PBS) Amies Buffer MDK-NA01,MDK-NA02,MDK-NA03 Vacuum Blood Collection Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KDT	Container, Specimen Mailer And Storage, Sterile	Pathology	Class 1	864.3250	2020-03-23
KXF	Applicator, Absorbent Tipped, Non-Sterile	General Hospital	Class 1	880.6025	2020-08-22
JSG	Culture Media, Non-Selective And Non-Differential	Microbiology	Class 1	866.2300	2020-09-20
PPM	General Purpose Reagent	Pathology	Class 1	864.4010	2020-07-27
EPE	Brush, Cleaning, Tracheal Tube	Anesthesiology	Class 1	868.5795	2025-08-19
KIP	Formulations, Balanced Salt Solutions	Hematology	Class 1	864.2875	2020-07-28
GIO	Tube, Collection, Capillary Blood	Hematology	Class 1	864.6150	2025-12-01

Official Correspondent

CHUN HONG Wang

US Agent Details

Peter Yang Business: JIAMEI CONSULTING INC. Email: info@jiameiconsulting.com Phone: (310) 2168437

Related Public Records

Same Entity

MEDICO 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
K880142	Hardy Media	TSA W/LEC. & TWEEN. 80	1988-03-30

Similar Registrations

Registration Number	Establishment Name	Location
3027605742	Xiamen Zhiyuan Medical Technology Co., Ltd.	XIAMEN Fujian, CN
2320762	DEROYAL INDUSTRIES, INC.	NEW TAZEWELL, TN, US
3010420046	CITOTEST Labware Manufacturing CO., LTD.	Haimen Jiangsu, CN
3044466317	MEDINOVA GROUP CO.	Laguna Beach, CA, US
1055236	DEROYAL INDUSTRIES, INC.	NEW TAZEWELL, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016710934. Last updated year: 2026. Please use registration number 3016710934 when referencing this establishment in official correspondence.