FDA applicant

Morpheus AG

Spaichingen, DE3 decisions2021–20230 recalls

FDA records 3 decisions for Morpheus AG (Spaichingen, DE) from 2021 to 2023: 3 510(k) clearances. All are in product code HAE (Rongeur, Manual). Its devices cite 4 predicates, 3 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, neurology panel, where it files most

How often FDA has decided Morpheus AG’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2021high 1 (2021) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Morpheus AG by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Morpheus AG’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Morpheus”

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

Morpheus Imaging, Inc. 1

Morpheus AG

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Morpheus”