RegWardenFDA facility compliance records
Facility

Innomedic GmbH

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

Activity by year

FDA actions on record by year2020: 1 recalls20172018201912020202120222023202420252026
  • Recalls (1)

Devices registered here (2)

  • Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
    Product code KTT (opens in a new tab) · Class II · Orthopedic · 21 CFR 888.3030
  • Software For Diagnosis/Treatment
    Product code OSN (opens in a new tab) · Class II · Orthopedic · 21 CFR 888.3030

Recalls & enforcement

  • Class IITerminated2020-06-16
    One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm).

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. “Innomedic GmbH (FEI 3013510178) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3013510178-innomedic-gmbh/

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