Hmd Hk L T D

FDA Filings

This page includes the latest FDA filings for Hmd Hk 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 Number3013947315
FEI Number3013947315
NameAnny Zhao
Owner & OperatorHMD HK Ltd
Contact AddressUnit 2911, One Midtown, 11 Hoi Shing Roa
HK HK-NA 852 HK
Official Correspondent
  • Andy Hasbun
  • 852-2-3694848-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4951 netarts hwy west
Tillamook, OR 97141 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Anny Zhao [HMD HK Ltd]
Disposable Specula2018-11-22
Anny Zhao [HMD HK Ltd]
HMD Caliper2018-11-06
Anny Zhao [HMD HK Ltd]
HMD Stethoscope2018-05-31
Anny Zhao [HMD HK Ltd]
HMD Ophthalmoscope2018-05-31
Anny Zhao [HMD HK Ltd]
HMD Sensory Hearing Screener2018-05-31
Anny Zhao [HMD HK Ltd]
HMD Otoscope2018-05-31

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