Guolong Shenzhen High Technology Co L T D

FDA Filings

This page includes the latest FDA filings for Guolong Shenzhen High Technology Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3009746042
• FEI Number: 3009746042
• Name: GuoLong (Shenzhen) High Technology Co., Ltd
• Owner & Operator: GuoLong (Shenzhen) High Technology Co., Ltd.
• Contact Address: Floor 1 Bldg E Dehuida Ind Park No. 237 Xikeng Rd, Guanlan St. Longhua New Dist; Shenzhen CN-44 Guangdong 518110 CN
• US Agent:
  • David Lennarz
  • Registrar Corp
  • 757 2240177
  • 757 2240179
  • david.lennarz@registrarcorp.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Floor 1 Bldg E Dehuida Ind Park No. 237 Xikeng Rd, Guanlan St. Longhua New Dist; Shenzhen Guangdong, 518110 CN
• Establishment Type:
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
ITC GuoLong (Shenzhen) High Technology Co., Ltd [GuoLong (Shenzhen) High Technology Co., Ltd.]	Norco	2018-12-31
OHY GuoLong (Shenzhen) High Technology Co., Ltd [GuoLong (Shenzhen) High Technology Co., Ltd.]	Norco	2017-12-21
GWI GuoLong (Shenzhen) High Technology Co., Ltd [GuoLong (Shenzhen) High Technology Co., Ltd.]	Touch-Test	2012-12-10
ILD GuoLong (Shenzhen) High Technology Co., Ltd [GuoLong (Shenzhen) High Technology Co., Ltd.]	Oxo	2012-07-26