FDA applicant

Micrus Design Technology, Inc.

Miami, FL1 decision2007–20070 recalls

FDA records 1 decision for Micrus Design Technology, Inc. (Miami, FL) in 2007: 1 510(k) clearance. All are in product code DYB (Introducer, Catheter). 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 Micrus Design Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Micrus”

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

Micrus Endovascular Corporation 23 Micrus Corp. 6

Micrus Design Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Micrus”