510(k) Report

FDA applicant

Senair-Mot

Orange, CA2 decisions1984–19900 recalls

FDA records 2 decisions for Senair-Mot (Orange, CA) from 1984 to 1990: 2 510(k) clearances. Most are in product codes JEW (Tip, Rubber, Oral Hygiene) and EJI (Syringe, Cartridge). 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 Senair-Mot’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Senair-Mot since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • JEWTip, Rubber, Oral Hygiene1decision
  • EJISyringe, Cartridge1decision

What has FDA decided for it lately?

All 2 as Senair-Mot →