FDA applicant

Brahms Aktiengesellschaft

Beltsville, MD2 decisions2005–20080 recalls

FDA records 2 decisions for Brahms Aktiengesellschaft (Beltsville, MD) from 2005 to 2008: 2 510(k) clearances. All are in product code NTM (Antigen, Inflammatory Response Marker, Sepsis). Its devices cite 2 predicates, 1 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, microbiology panel, where it files most

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

FDA decisions per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Brahms Aktiengesellschaft’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 “Brahms”

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

Brahms Diagnostica, LLC 6 Brahms GmbH 2 Brahms GmbH, Part of Thermo Fisher Scientific 1 B.R.A.H.M.S GmbH, Part of Thermo Fisher 1

Brahms Aktiengesellschaft

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Brahms”