FDA applicant

Tyco Electronics Corporation

Wilsonville, OR1 decision2010–20100 recalls

FDA records 1 decision for Tyco Electronics Corporation (Wilsonville, OR) in 2010: 1 510(k) clearance. All are in product code DSA (Cable, Transducer And Electrode, Patient…). Its devices cite 1 predicate, 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, cardiovascular panel, where it files most

How often FDA has decided Tyco Electronics Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Tyco Electronics Corporation by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Tyco”

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

Tyco Healthcare 14 Tyco Healthcare Group LP 6 Tyco Healthcare/Kendall 4 Tyco Healthcare Nancy 2 Tyco Intl. (Us), Inc. 1 Tyco Healthcare Deutschaland GmbH 1

Tyco Electronics Corporation

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Tyco”