FDA applicant

Micro-Mega

France, FR2 decisions1994–19970 recalls

FDA records 2 decisions for Micro-Mega (France, FR) from 1994 to 1997: 2 510(k) clearances. Most are in product codes EKS (File, Pulp Canal, Endodontic) and EGS (Handpiece, Contra- And Right-Angle Attachment…). 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 Micro-Mega’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micro-Mega since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Micro-Mega’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

Micro-Mega

Which product codes does it file in?

What has FDA decided for it lately?