FDA applicant

Inter Medical Medizintechnik GmbH

Luebbecke, DE3 decisions2005–20230 recalls

FDA records 3 decisions for Inter Medical Medizintechnik GmbH (Luebbecke, DE) from 2005 to 2023: 3 510(k) clearances. Most are in product codes KPS (System, Tomography, Computed, Emission) and IYX (Camera, Scintillation (Gamma)). 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, radiology panel, where it files most

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

FDA decisions per year

1in 2023

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Inter Medical Medizintechnik GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Inter”

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

Inter-Med, Inc. 12 Inter-Med/Vista Dental Products 6 Inter Med Industries, Inc. 3 Inter Science Institute 3 Inter-Os Technologies 2 Inter Continental Health Care 2 Inter-Asia Co., Inc. 1 Inter-Pal GmbH 1 Inter-Med / Vista Dental 1 Inter-Continental Industries Sdn Bhd 1

Inter Medical Medizintechnik GmbH

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 “Inter”