Hangzhou Kebo Orthopedic Rehabilitation Equipment L T D

FDA Filings

This page includes the latest FDA filings for Hangzhou Kebo Orthopedic Rehabilitation Equipment 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 Number3014579162
FEI Number3014579162
NameFiona Chan
Owner & OperatorHangzhou Kebo Orthopedic Rehabilitation Equipment Limited
Contact AddressNo.8 Houshan Road Wuchang Street
Hangzhou CN-33 Zhejiang 310000 CN
Official Correspondent
  • Shuai Jin
  • 86-571-8524-2297
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address6050 W EASTWOOD AVE APT 201
Chicago, IL 60630 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Fiona Chan [Hangzhou Kebo Orthopedic Rehabilitation Equipment Limited]
Shoulder brace2019-08-27
Fiona Chan [Hangzhou Kebo Orthopedic Rehabilitation Equipment Limited]
Ankle brace,Foot Brace2019-08-27
Fiona Chan [Hangzhou Kebo Orthopedic Rehabilitation Equipment Limited]
Knee brace,Hip Ankle Knee brace2019-08-27
Fiona Chan [Hangzhou Kebo Orthopedic Rehabilitation Equipment Limited]
Neck brace,Cervical collar bace2019-08-27
Fiona Chan [Hangzhou Kebo Orthopedic Rehabilitation Equipment Limited]
Elbow brace,Wrist brace,Waist brace,Hip brace2019-08-27
Fiona Chan [Hangzhou Kebo Orthopedic Rehabilitation Equipment Limited]
Splint,Hinge,Lock2019-08-27

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