Colonic Plus

FDA Filings

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

FDA Registration(s)
Registration Number3006124873
FEI Number3006124873
NameCOLONIC PLUS
Owner & OperatorCOLONIC PLUS
Contact Address73925 HWY 111 Suite L
Palm Desert CA 92260 US
Official Correspondent
  • ROSA - ALVAREZ
  • x-760-3400720-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address73-925 HWY 111, STE L
PALM DESERT, CA 92260 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
COLONIC PLUS
Colonic Plus Regular, Small, and Straight Shape Hydrokits2019-01-09
Colonic Plus
Colonic Plus Regular, Small, And Straight Shape Hydrokit2018-06-01

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2019082140872Ningpo ,China (Mainland) -> Long Beach, CaliforniaEVA TUBE PVC TUBE125 CTN
2019061135636Yantian,China (Mainland) -> Los Angeles, CaliforniaPLASTIC FILM1 PKG
2019061046600Yantian,China (Mainland) -> Los Angeles, CaliforniaPACKING MACHINE .1 PKG
2019031142984Ningpo ,China (Mainland) -> Los Angeles, CaliforniaEVA TUBE,PVC TUBE90 CTN
2018091961156Ningpo ,China (Mainland) -> Los Angeles, CaliforniaEVA TUBE25 CTN
2018091750295Yantian,China (Mainland) -> Los Angeles, CaliforniaPOLY BAG FOR PACKAGING THIS SHIPMENT CONTAIN S NO SOLID WOOD PACKING MATERIALS17 CTN

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.