Proxy Biomedical L T D

FDA Filings

This page includes the latest FDA filings for Proxy Biomedical 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 Number3004859928
FEI Number3004859928
NameElaine Duncan
Owner & OperatorProxy Biomedical Ltd
Contact AddressCoilleach Spiddal
Co. Galway IE-NOTA H91 C2NF IE
Official Correspondent
  • Adrienne Tierney
  • 353-91-896900-934
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address415 Valley View Trail
Houlton, WI 54082 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Proxy Biomedical Ltd.
VitaMESH Macroporous PP Surgical Mesh2018-04-30
Elaine Duncan [Proxy Biomedical Ltd]
Upsylon Y Mesh Kit with Colpassist Vaginal Positioning Device2013-07-03
Elaine Duncan [Proxy Biomedical Ltd]
Colpassist Vaginal Positioning Device2013-05-02
Elaine Duncan [Proxy Biomedical Ltd]
Upsylon Traditional Y mesh2013-03-19
PROXY BIOMEDICAL LTD.
VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH2011-05-13
Elaine Duncan [Proxy Biomedical Ltd]
Polyform Synthetic Mesh2007-11-29
PROXY BIOMEDICAL LTD.
VITAMESH MACROPOROUS PP SURGICAL MESH2006-03-28
PROXY BIOMEDICAL LTD.
MODIFICATION TO MOTIFMESH SOFT TISSUE PATCH2005-08-11
PROXY BIOMEDICAL LTD.
POLYFORM SYNTHETIC MESH2005-06-17
PROXY BIOMEDICAL LTD.
MOTIFMESH SOFT TISSUE PATCH2005-05-20

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