FDA applicant

Vitrolife AB/Scandinavian Ivf Sciences AB

Washington, DC7 decisions2000–20000 recalls

FDA records 7 decisions for Vitrolife AB/Scandinavian Ivf Sciences AB (Washington, DC) in 2000: 7 510(k) clearances. All are in product code MQL (Media, Reproductive). 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 Vitrolife AB/Scandinavian Ivf Sciences AB’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vitrolife AB/Scandinavian Ivf Sciences AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vitrolife AB/Scandinavian Ivf Sciences AB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vitrolife AB/Scandinavian Ivf Sciences…’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 “Vitrolife”

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

Vitrolife Sweden AB 38 Vitrolife AB 5 Vitrolife A/S 4

Vitrolife AB/Scandinavian Ivf Sciences AB

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 “Vitrolife”