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Lifelines Neuro Company

United Statesfrom the FDA registration address FDA establishment FEI 3015491430

Devices
0
Registrations
FDA
FDA recalls
2

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3015491430
Address
900 East Main Street, Louisville, KY, 40206

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 2
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0

  • 2019

    • 11 Oct 2019 Z-0722-2020 Class II Terminated Potential for one of the four temporal electrode cables used in with the ElectroTek EEG system having incorrect placement labels which could lead to incorrect placement of electrode for an EEG study. Distribution: US Nationwide distribution in the states of TX, TN, NC. Submission number: K170441
    • 11 Oct 2019 Z-0723-2020 Class II Terminated Potential for one of the four temporal electrode cables used in with the ElectroTek EEG system having incorrect placement labels which could lead to incorrect placement of electrode for an EEG study. Distribution: US Nationwide distribution in the states of TX, TN, NC. Submission number: K170441

This is an FDA establishment record without devices in deviCERTS.