Celestica Oregon L L C

FDA Filings

This page includes the latest FDA filings for Celestica Oregon L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009039038
FEI Number3009039038
NameCELESTICA OREGON LLC
Owner & OperatorCelestica Oregon LLC
Contact Address18870 NE Riverside Pkwy
Portland OR 97230 US
Official Correspondent
  • Troy Boteilho
  • x-971-4095172-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address18870 NE Riverside Pkwy
Portland, OR 97230 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
CELESTICA OREGON LLC
VPS Rhythm Device with Optional TipTracker Technology2017-01-20
CELESTICA OREGON LLC
Percutaneous, implanted, long-term intravascular catheter2016-12-20

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020092914590Singapore,Singapore -> Tacoma, WashingtonPDU ASSY M-SERIES S-SPEC 3W SEM F/CD1 CRT
2020092821226Shanghai ,China (Mainland) -> Tacoma, WashingtonPLASTIC COVER3 PKG
2020092821230Shanghai ,China (Mainland) -> Tacoma, WashingtonRELIEF VALVES11 PKG
2020092816079Singapore,Singapore -> Tacoma, WashingtonPDU ASSY M-SERIES S-SPEC 3W SEM F/CD1 CRT
2020092630199Shanghai ,China (Mainland) -> Tacoma, WashingtonRELIEF VALVES11 PKG
2020092630195Shanghai ,China (Mainland) -> Tacoma, WashingtonPLASTIC COVER3 PKG
202009251874Singapore,Singapore -> Tacoma, WashingtonWOODEN CASES17 BOX
202009243350Shanghai ,China (Mainland) -> Seattle, WashingtonRELIEF VALVES5 PKG

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