FDA applicant

Instrumentarium Dental, Palodex Group OY

Tuusula, FI5 decisions2007–20140 recalls

FDA records 5 decisions for Instrumentarium Dental, Palodex Group OY (Tuusula, FI) from 2007 to 2014: 5 510(k) clearances. All are in product code MUH (System, X-Ray, Extraoral Source, Digital). Its devices cite 6 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, dental panel, where it files most

How often FDA has decided Instrumentarium Dental, Palodex Group OY’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2007high 1 (2007) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Instrumentarium Dental, Palodex Group OY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Instrumentarium Dental, Palodex Group OY’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 “Instrumentarium”

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

Instrumentarium Imaging, Inc. 24 Instrumentarium Corp. 20 Instrumentarium Corp. Imaging Division 3 Instrumentarium-Datex 2 Instrumentarium Dental, Inc. 1

Instrumentarium Dental, Palodex Group OY

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 “Instrumentarium”