510(k) Report

FDA applicant

Mht Optic Research AG

Niederhasli, CH1 decision2002–20020 recalls

FDA records 1 decision for Mht Optic Research AG (Niederhasli, CH) in 2002: 1 510(k) clearance. All are in product code EIA (Unit, Operative Dental). 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 Mht Optic Research AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mht Optic Research AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mht Optic Research AG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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