FDA applicant

Teledyne Avionics Div. of Teledyne

Charlottesville, VA13 decisions1979–19860 recalls

FDA records 13 decisions for Teledyne Avionics Div. of Teledyne (Charlottesville, VA) from 1979 to 1986: 13 510(k) clearances. Most are in product codes ETY (Tester, Auditory Impedance) and EWO (Audiometer). 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 Teledyne Avionics Div. of Teledyne’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teledyne Avionics Div. of Teledyne since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Teledyne Avionics Div. of Teledyne by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Teledyne”

FDA records each applicant name separately; these may or may not be the same firm.

Teledyne, Inc. 10 Teledyne Water Pik 9 Teledyne Getz 5 Teledyne Densco 4 Teledyne Analytical Instruments 3 Teledyne Electronic Technologies 2 Teledyne Brown Engineering 2

Teledyne Avionics Div. of Teledyne

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Teledyne”