RegWardenFDA facility compliance records
Facility

Aligntech de Mexico S, de R. L. de C. V.

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

Activity by year

FDA actions on record by year2022: 1 recalls20172018201920202021120222023202420252026
  • Recalls (1)

Devices registered here (1)

  • Cleaner, Ultrasonic, Medical Instrument
    Product code FLG (opens in a new tab) · Class I · General Hospital · 21 CFR 880.6150

Recalls & enforcement

  • Class IICompleted2022-12-05
    3D orthodontic planning software has a defect that leads to an issue where incorrect number of aligners may be produced (less or greater than the doctor requested) and incorrect packaging is provided.

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. “Aligntech de Mexico S, de R. L. de C. V. (FEI 3007527669) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007527669-aligntech-de-mexico-s-de-r-l-de-c-v/

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