FDA.reportPublic FDA data

GREEN OR LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30214778083021477808GREEN OR LLC1N2026-01-0117685 Juniper Path Ste 314 Lakeville MN US 55044

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3010611690742714K173741Reprocessed ArthoCare Ablation WandNUJ2018-03-05
3010611404102583K173740Reprocessed DePuy Mitek Ablation WandNUJ2018-03-19
3010612018852808K172647Reprocessed ArthroCare ENT CoblatorNUJ2018-02-21
3010611423769188K172097Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar SleevesNLM2017-10-06
3010611594354517K172093Reprocessed Covidien TrocarNLM2017-10-05
3010611611087180K172092Reprocessed Shavers/BursHRX2017-10-04
3010611003744939
3010611013137373
3010611147287605
3010611155228525
3010611362468655
3010611443946538
3010611454434048
3010611463323764
3010611463773588
3010611470112663
3010611474486824
3010611512579488
3010611593740327
3010611605420640
3010611699649928
3010611752624291
3010611894792228
3010611931936843
3010612029363192
3010612063251050

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NUJ32018-03-19
NLM22017-10-06
HRX12017-10-04

GUDID#