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Enchroma, Inc.

Country not established FDA establishment FEI 3009455348

Devices
0
Registrations
FDA
FDA recalls
11 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3009455348
Address
2001 Addison St Ste 300, Berkeley, CA, 94704

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 1
  • 2025 0
  • 2026 0

  • 2024

    • 6 Sep 2024 Z-0488-2025 Class II Ongoing Safety glasses with Rx indoor universal lenses fail to meet high impact safety specifications, which may not provide adequate protection against impact, posing a risk of eye injury. Distribution: Worldwide distribution: US (nationwide): IL, OH, NC, IA, AL, SC, NJ, TX, CO, PA, FL, MI, NY, DU, NM, CA, NH, MT, WV, KY,…
      Full distribution text Worldwide distribution: US (nationwide): IL, OH, NC, IA, AL, SC, NJ, TX, CO, PA, FL, MI, NY, DU, NM, CA, NH, MT, WV, KY, OR, MA, WI, VA, AZ and OUS (foreign): United Arab Emirates, Japan, and Canada.

This is an FDA establishment record without devices in deviCERTS.