510(k) Report

FDA applicant

Eare Consulting Service

Eilat, IL4 decisions1994–19970 recalls

FDA records 4 decisions for Eare Consulting Service (Eilat, IL) from 1994 to 1997: 4 510(k) clearances. Most are in product codes CCW (Laryngoscope, Rigid) and LLN (Device, Vibration Threshold Measurement). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, anesthesiology panel, where it files most

How often FDA has decided Eare Consulting Service’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eare Consulting Service since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Eare Consulting Service 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?

  • CCWLaryngoscope, Rigid1decision
  • LLNDevice, Vibration Threshold Measurement1decision
  • HRXArthroscope1decision
  • DZPInstrument, Diamond, Dental1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K950592Accessories Foe Orthopedic Surgical ProceduresEare Consulting Service · 19951cites it

What has FDA decided for it lately?

  • K970180Vsa 3000 Vibratoryn Sensory AnalyzerEare Consulting Service · 1997
  • K950592Accessories Foe Orthopedic Surgical ProceduresEare Consulting Service · 1995
  • K944428Lite-BladeEare Consulting Service · 1994
  • K934981Dental DrillEare Consulting Service · 1994

All 4 as Eare Consulting Service →