Lantor Uk L T D

FDA Filings

This page includes the latest FDA filings for Lantor Uk 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 Number8021899
FEI Number6664
NameLANTOR (UK), LTD.
Owner & OperatorLANTOR (UK), LTD.
Contact AddressST. HELENS RD. --
BOLTON GB-MAN Manchester BL3 3PR GB
Official Correspondent
  • Scott Bainbridge
  • 44-1244-855000-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressST. HELENS RD.
BOLTON Bolton, BL3 3PR GB
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
LANTOR (UK), LTD.
SurePress Absorbent Padding2013-01-25
LANTOR (UK), LTD.
PROFORE Wound Contact Layer ?TRICOTEX2012-06-27
LANTOR (UK), LTD.
LANTOR CUBE2006-04-10

Related Finance Registrations
NCAGE CodeK7465LANTOR (UK) LTD
CAGE CodeK7465LANTOR (UK) LTD
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
202009188546London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING516 PCS
202009189900London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING1050 CTN
2020091225846London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING1050 CTN
2020091222497London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING516 PCS
2020082028222London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING516 PCS
2020082031397London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING1050 PCS
2020080634647London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING1050 CTN
2020071528621London,United Kingdom -> Houston, TexasORTHOPAEDIC PADDING516 CTN
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