FDA applicant

Nexstim Oyj

Helsinki, FI2 decisions2026–20260 recalls

FDA records 2 decisions for Nexstim Oyj (Helsinki, FI) in 2026: 2 510(k) clearances. All are in product code OBP (Transcranial Magnetic Stimulator). Its devices cite 2 predicates, 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, neurology panel, where it files most

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

FDA decisions per year

2in 2026

2026high 2 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

Planning a device like Nexstim Oyj’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 “Nexstim”

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

Nexstim OY 4

Nexstim Oyj

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Nexstim”