Kerecis Arlington

FDA Filings

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

FDA Registration(s)
Registration Number3013281127
FEI Number3013281127
NameKerecis Arlington
Owner & OperatorKerecis ehf
Contact AddressEyrargata 2
Isafjordur IS-4 Vestfiroir 400 IS
Official Correspondent
  • Fertram Sigurjonsson
  • 354-8-494960-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address2200 Clarendon Boulevard Suite 1400A
Arlington, VA 22201 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198

FDA Filings

Device
Company
DeviceDate
Kerecis Arlington [Kerecis ehf]
MariGen Wound Extra2019-10-21
Kerecis Arlington [Kerecis ehf]
Kerecis Burn2019-10-21
Kerecis Arlington [Kerecis ehf]
Marigen Omega32013-11-12
Kerecis Arlington [Kerecis ehf]
Marigen Omega3 Wound2013-11-12
Kerecis Arlington [Kerecis ehf]
MariGen2013-11-12
Kerecis Arlington [Kerecis ehf]
MariGen Wound2013-11-12
Kerecis Arlington [Kerecis ehf]
Kerecis Omega32013-11-12
Kerecis Arlington [Kerecis ehf]
Kerecis Omega3 Wound2013-11-12
Kerecis Arlington [Kerecis ehf]
Alphaplex with MariGen Wound2013-11-12

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