510(k) Report

FDA applicant

Micomed GmbH

Fullerton, CA2 decisions1999–20000 recalls

FDA records 2 decisions for Micomed GmbH (Fullerton, CA) from 1999 to 2000: 2 510(k) clearances. Most are in product codes MNI (Orthosis, Spinal Pedicle Fixation) and KWQ (Appliance, Fixation, Spinal Intervertebral Body). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Micomed GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micomed GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micomed GmbH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MNIOrthosis, Spinal Pedicle Fixation1decision
  • KWQAppliance, Fixation, Spinal Intervertebral Body1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K982006Micomed - Halm Zielke InstrumentationMicomed GmbH · 19991cites it

What has FDA decided for it lately?

  • K991862Micomed Posterior Doublerod System (MPDS)Micomed GmbH · 2000
  • K982006Micomed - Halm Zielke InstrumentationMicomed GmbH · 1999

All 2 as Micomed GmbH →

Other applicant names beginning “Micomed”

FDA records each applicant name separately; these may or may not be the same firm.

Micomed Ortho GmbH 2