RegWardenFDA facility compliance records
Facility

BRIUS Technologies Inc.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2022: 1 recalls; 2024: 1 inspections201720182019202020211202220231202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

Recalls & enforcement

  • Class IITerminated2022-02-07
    Pontics, brackets, and customized orthodontic appliances were sold and distributed prior to completing the standard design control process, being documented, and released.

FDA inspections (1)

  • VAI2024-10-07
    Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “BRIUS Technologies Inc. (FEI 3014680924) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3014680924-brius-technologies-inc/

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