Kmihh L T D

FDA Filings

This page includes the latest FDA filings for Kmihh 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 Number3011820414
FEI Number3011820414
NameArye Shahar
Owner & OperatorKMIHH LTD
Contact Address2 Ha-Khayil St
Kdumim IL-M HaMerkaz 4485600 IL
Official Correspondent
  • Or Ramot
  • 972-54-4319453-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address9 Florida Park Drive N
Palm Coast, FL 32137 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Arye Shahar [KMIHH LTD]
MagicAir2020-01-21
Arye Shahar [KMIHH LTD]
Magic Mirror2020-01-21
KMIHH Ltd
Le'Pen2019-04-01

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