FDA applicant

Teledyne Analytical Instruments

City Of Industry, CA3 decisions2000–20031 recall

FDA records 3 decisions for Teledyne Analytical Instruments (City Of Industry, CA) from 2000 to 2003: 3 510(k) clearances. All are in product code CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). 1 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 Teledyne Analytical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teledyne Analytical Instruments since 2007.

Recalls per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Teledyne Analytical Instruments 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 Avionics Div. of Teledyne 13 Teledyne, Inc. 10 Teledyne Water Pik 9 Teledyne Getz 5 Teledyne Densco 4 Teledyne Electronic Technologies 2 Teledyne Brown Engineering 2

Teledyne Analytical Instruments

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Teledyne”