FDA applicant

Moeller Medical GmbH & Co. KG

Coto De Caza, CA2 decisions2006–20080 recalls

FDA records 2 decisions for Moeller Medical GmbH & Co. KG (Coto De Caza, CA) from 2006 to 2008: 2 510(k) clearances. All are in product code QPB (System, Suction, Lipoplasty For Removal). Its devices cite 5 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 and plastic surgery panel, where it files most

How often FDA has decided Moeller Medical GmbH & Co. KG’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Moeller”

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

Moeller Microsurgical, Inc. 2 Moeller Chemicals, Inc. 1

Moeller Medical GmbH & Co. KG

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Moeller”