FDA applicant

Labotect Labor-Technik Gottingen

Gottingen, DE3 decisions2000–20020 recalls

FDA records 3 decisions for Labotect Labor-Technik Gottingen (Gottingen, DE) from 2000 to 2002: 3 510(k) clearances. Most are in product codes MFD (Cannula, Intrauterine Insemination) and MQE (Needle, Assisted Reproduction). Its devices cite 4 predicates, 0 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Labotect Labor-Technik Gottingen’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Labotect Labor-Technik Gottingen since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Labotect Labor-Technik Gottingen by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Labotect Labor-Technik Gottingen’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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Labotect Labor-Technik Gottingen

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?