510(k) Report

FDA applicant

Hnl Technologies

San Mateo, CA1 decision1998–19980 recalls

FDA records 1 decision for Hnl Technologies (San Mateo, CA) in 1998: 1 510(k) clearance. All are in product code LWF (Dilator, Nasal). 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, ear, nose and throat panel, where it files most

How often FDA has decided Hnl Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hnl Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hnl Technologies 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?

  • LWFDilator, Nasal1decision

What has FDA decided for it lately?

  • K982929Maxair Nasal Dilator SystemHnl Technologies · 1998

The one decision as Hnl Technologies →