Croom Precision Tooling L T D

FDA Filings

This page includes the latest FDA filings for Croom Precision Tooling 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 Number3009185591
FEI Number3009185591
NameCROOM PRECISION TOOLING LTD
Owner & OperatorCROOM PRECISION TOOLING LTD
Contact AddressSFADCO ENTERPRISE CENTRE CROOM
LIMERICK IE-LK Limerick NA IE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressSFADCO ENTERPRISE CENTRE CROOM
LIMERICK Limerick, NA IE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
CROOM PRECISION TOOLING LTD
HOWMEDICA OSTEONICS? MODULAR ROTATING HINGE KNEE2013-01-30
CROOM PRECISION TOOLING LTD
HOWMEDICA KINEMAX PLUS TOTAL KNEE SYSTEM2013-01-30
CROOM PRECISION TOOLING LTD
KINEMAX SUPERSTABILIZER TOTAL KNEE SYSTEM2013-01-30

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