Pharmelite

FDA Filings

This page includes the latest FDA filings for Pharmelite. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3003950102
FEI Number3003950102
NameGlen Feye
Owner & OperatorPharmelite
Contact Address63 Jalan Pemimpin No 02-07 Pemimpin Industrial Building
Pemimpin SG-NOTA 577219 SG
Official Correspondent
  • Poon K Tham
  • 65-6353-9128-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3234 Ibis Street
San Diego, CA 92103 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Glen Feye [Pharmelite]
Spacelabs Blood Pressure Monitoring Cuff Covers2017-08-12

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