510(k) Report

FDA applicant

Henning Knudsen Engineering A/S

Birkerod, DK1 decision1999–19990 recalls

FDA records 1 decision for Henning Knudsen Engineering A/S (Birkerod, DK) in 1999: 1 510(k) clearance. All are in product code MQG (Accessory, Assisted Reproduction). 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 Henning Knudsen Engineering A/S’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Henning Knudsen Engineering A/S since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Henning Knudsen Engineering A/S 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?

  • MQGAccessory, Assisted Reproduction1decision

What has FDA decided for it lately?

  • K991229K-Systems Work Stations, Type L-13W, L-13E, L-13ES, L-13ET, L-13EM, L-23, L-23E, L-24, L-24E, L-25, L-25E…Henning Knudsen Engineering A/S · 1999

The one decision as Henning Knudsen Engineering A/S →