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.
| Registration Number | 3013947315 |
| FEI Number | 3013947315 |
| Name | Anny Zhao |
| Owner & Operator | HMD HK Ltd |
| Contact Address | Unit 2911, One Midtown, 11 Hoi Shing Roa HK HK-NA 852 HK |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 4951 netarts hwy west Tillamook, OR 97141 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Anny Zhao [HMD HK Ltd] | Disposable Specula | 2018-11-22 |
Anny Zhao [HMD HK Ltd] | HMD Caliper | 2018-11-06 |
Anny Zhao [HMD HK Ltd] | HMD Stethoscope | 2018-05-31 |
Anny Zhao [HMD HK Ltd] | HMD Ophthalmoscope | 2018-05-31 |
Anny Zhao [HMD HK Ltd] | HMD Sensory Hearing Screener | 2018-05-31 |
Anny Zhao [HMD HK Ltd] | HMD Otoscope | 2018-05-31 |