510(k) Report

FDA applicant

Lmt Lammers Medical Technology GmbH

Luebeck, DE2 decisions2003–20060 recalls

FDA records 2 decisions for Lmt Lammers Medical Technology GmbH (Luebeck, DE) from 2003 to 2006: 2 510(k) clearances. All are in product code FPL (Incubator, Neonatal Transport). Its devices cite 2 predicates, 1 of them its own earlier devices. 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, general hospital panel, where it files most

How often FDA has decided Lmt Lammers Medical Technology GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lmt Lammers Medical Technology GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lmt Lammers Medical Technology 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?

  • FPLIncubator, Neonatal Transport2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 1 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.

  • K033565LMT Nomag IC 1,5Lmt Lammers Medical Technology GmbH · 20032cite it
  • K062052LMT Nomag IC 3.0Lmt Lammers Medical Technology GmbH · 20061cites it

What has FDA decided for it lately?

  • K062052LMT Nomag IC 3.0Lmt Lammers Medical Technology GmbH · 2006
  • K033565LMT Nomag IC 1,5Lmt Lammers Medical Technology GmbH · 2003

All 2 as Lmt Lammers Medical Technology GmbH →