FDA.report

KEOS

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30139210693013921069KEOS1N2026-01-011824 COLONIAL VILLAGE LN Lancaster PA US 17601

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2113892011897633K212450Keos Anterior Cervical Interbody Fusion Device SystemODP2022-06-06
2113891846686499K193174Keos Lumbar IBFDMAX2019-12-16
2113891722810490K163386Keos Lumbar IBFDMAX2017-04-10
2113891176321490K160631Keos Lumbar IBFDMAX2016-07-15
2113891438577233
2113892045693097

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
MAX32019-12-16
ODP12022-06-06

PMN

GUDID

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