BenQ Materials Corporation

FDA Filings

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

FDA Registration(s)
Registration Number3010256218
FEI Number3010256218
NameDavid Lennarz
Owner & OperatorBENQ MATERIALS CORPORATION
Contact Address29, Jianguo E. Rd.
Gueishan TW-TAO Taoyuan 33341 TW
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address144 Research Drive
Hampton, VA 23666 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
BenQ Materials Corporation
Anscare SIMO Negative Pressure Wound Therapy (NPWT) System2020-05-04
BENQ MATERIALS CORPORATION
AnsCare ChitoClot Pad2015-11-05
BENQ MATERIALS CORPORATION
AnsCare ChitoClot Gauze (prescription Use), AnsCare ChitoClot Gauze (over-the-counter Use)2015-05-08
David Lennarz [BENQ MATERIALS CORPORATION]
DermaAngel Acne Patch2014-01-23

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