FDA applicant

Imds Operations B.V.

Roden, NL8 decisions2012–20250 recalls

FDA records 8 decisions for Imds Operations B.V. (Roden, NL) from 2012 to 2025: 8 510(k) clearances. All are in product code DQY (Catheter, Percutaneous). Since 2016 its 510(k)s took a median of 178 days from receipt to decision, against 114 for FDA’s reviews in the same codes and years. Its devices cite 8 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, cardiovascular panel, where it files most

How often FDA has decided Imds Operations B.V.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2012high 2 (2020) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Imds Operations B.V. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Imds Operations B.V.’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 “Imds”

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

Imds (Innovative MEdical Device Systems) - Leis ME 1 IMDS Operation B.V. 1

Imds Operations B.V.

Which product codes does it file in?

How long do its 510(k) reviews take?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Imds”