RegWardenFDA facility compliance records
Company

XINTEC CORPORATION DBA CONVERGENT LASER TECHNOLOGIES

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

Recalls by year

FDA actions on record by year2017: 2 recalls22017201820192020202120222023202420252026
  • Recalls (2)

Registered facilities (1)

Recalls & enforcement

  • Class IIITerminated2017-10-29
    It has been determined that a lot of fiber lasers were programmed incorrectly. As a result, the fibers from this lot will produce an error and will not allow the user to use the laser when it is plugged in.
  • Class IITerminated2017-06-23
    It has been determined that the reprocessing instructions may not provide sufficiently detailed information for the cleaning, disinfection and sterilization of the products listed below. The preliminary investigation indicates that validation data related to the reprocessing of t…

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “XINTEC CORPORATION DBA CONVERGENT LASER TECHNOLOGIES — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2938889-xintec-corporation-dba-convergent-laser-/

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