FDA applicant

At Medical Uab

Kaunas, LT2 decisions2014–20160 recalls

FDA records 2 decisions for At Medical Uab (Kaunas, LT) from 2014 to 2016: 2 510(k) clearances. 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 At Medical Uab’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — At Medical Uab by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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At Medical Uab

Which product codes does it file in?

What has FDA decided for it lately?