Remax Medi Tech Shenzhen Corp

FDA Filings

This page includes the latest FDA filings for Remax Medi Tech Shenzhen Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

Registration Number

3012234230

FEI Number

3012234230

Name

REMAX MEDI-TECH(SHENZHEN) CORPORATION

Owner & Operator

Remax Medi-tech(Shenzhen) Corporation

Contact Address

301, Building B, No. 7, Lane 1, Danfeng Street
Shenzhen CN-44 Guangdong 518000 CN

Official Correspondent

Fanny Cao
86-755-28012955-232

US Agent

Kevin Chen
Freedom Laser Therapy Inc.
714 6699888 105
daniel@freedomlasertherapy.com

Importing Logistics Registration

Importer	Freedom Laser Therapy, Inc.
Address	7815 Beverly Blvd., 3rd Fl. Los Angeles, CA 90036 UNITED STATES
Importer Type	brand owner

Registration Status

Initial Importer

Registration Expiration

2020-04-25

Registration Address

301, #21 Runtang industry zone, Fumin community, Fucheng street, Longhua district
Shenzhen Guangdong, 518000 CN

Establishment Type

Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 10859690003917 Remax Medi-Tech (Shenzhen) Corporation	iRestore	2023-08-09
GUDID 00859690003897 Remax Medi-Tech (Shenzhen) Corporation	iRestore	2022-03-29
GUDID 00859690003361 Remax medi-tech(Shenzhen)Corporation	iRestore	2018-09-12
PMN K151662 \| OAP REMAX MEDI-TECH(SHENZHEN) CORPORATION	iRestore Hair Growth System	2016-01-27