FDA applicant

Multicept, Aps.

2960 Rungsted Kyst,Denmark, DK2 decisions1985–19960 recalls

FDA records 2 decisions for Multicept, Aps. (2960 Rungsted Kyst,Denmark, DK) from 1985 to 1996: 2 510(k) clearances. Most are in product codes KXQ (Vibrator For Therapeutic Use, Genital) and LIL (Monitor, Penile Tumescence). 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 Multicept, Aps.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multicept, Aps. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Multicept, Aps.’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 “Multicept”

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

Multicept A/S 1

Multicept, Aps.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Multicept”