FDA applicant

Mermaid Care A/S

Norresundby, DK1 decision2019–20190 recalls

FDA records 1 decision for Mermaid Care A/S (Norresundby, DK) in 2019: 1 510(k) clearance. All are in product code BZK (Spirometer, Monitoring (W/Wo Alarm)). Its devices cite 1 predicate, 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, anesthesiology panel, where it files most

How often FDA has decided Mermaid Care A/S’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Mermaid Care A/S by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mermaid Care A/S’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 “Mermaid”

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

Mermaid Medical A/S 1

Mermaid Care A/S

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Mermaid”