Precimade

FDA Filings

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

FDA Registration(s)
Registration Number3011943495
FEI Number3011943495
NameKathy Trier
Owner & OperatorPrecimade
Contact Address161 Avenue Franklin Roosevelt
Decines FR-C Auvergne 69150 FR
Official Correspondent
  • David Demonceaux
  • 33-4-78766766-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address13465 Midway road
Dallas, TX 75244 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Kathy Trier [Precimade]
Humelock2017-05-21
Kathy Trier [Precimade]
Humelock2017-05-21
Kathy Trier [Precimade]
Humelock II2017-05-21
Kathy Trier [Precimade]
Humeris2017-05-18
Kathy Trier [Precimade]
Humeris2017-05-18
Kathy Trier [Precimade]
Humeris2017-05-18

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