FDA.reportPublic FDA data

KICO KNEE INNOVATION COMPANY

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30135524173013552417KICO KNEE INNOVATION COMPANY1N2026-01-01Unit 1, 25 Frenchs Forest Rd E Frenchs Forest New South Wales AU 2086

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2078281527073057K243980ARVIS Surgical Navigation SystemSBF2025-03-21
2078281801993200K243950ARVIS® ShoulderSBF2025-01-13
2078281502244875K242009360CAS KneeOLO2024-08-08
2078281330064996K240062ARVIS® ShoulderOLO2024-04-29
2078281978334772K223927360CASOLO2023-01-27
2078281247966557K213380360CASOLO2022-01-11
2078281455033896K203115ARVIS Surgical Navigation SystemOLO2021-07-14
2078281382026371K163405360KS Implant Positioning SystemLLZ2017-03-21
2078281310170950
2078281567048874
2078281585733674

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OLO52024-08-08
SBF22025-03-21
LLZ12017-03-21

PMN#

360CAS Knee

2024-08-08

Kico Knee Innovation Company Pty, Ltd.

360CAS

2023-01-27

Kico Knee Innovation Company Pty Limited

360CAS

2022-01-11

Kico Knee Innovation Company Pty Limited

GUDID#

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