510(k) Report

FDA applicant

Medsonic, Inc.

Farmingdale, NY1 decision1993–19931 recall

FDA records 1 decision for Medsonic, Inc. (Farmingdale, NY) in 1993: 1 510(k) clearance. All are in product code LFL (Instrument, Ultrasonic Surgical). 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

No FDA decision for Medsonic, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medsonic, Inc. 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?

  • LFLInstrument, Ultrasonic Surgical1decision

What has FDA decided for it lately?

  • K933559Alliger Ultrasonic Surgical SystemMedsonic, Inc. · 19931 recall

The one decision as Medsonic, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K933559LySonix 2000 Ultrasonic Surgical Systems, MODEL NO. LY-2000. --- Old labeling…Aug 13, 2003