FDA applicant

Sentron, Inc.

Federal Way, WA1 decision1992–19920 recalls

FDA records 1 decision for Sentron, Inc. (Federal Way, WA) in 1992: 1 510(k) clearance. All are in product code DXO (Transducer, Pressure, Catheter Tip). 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 Sentron, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sentron, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sentron, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Sentron”

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

Sentron Medical, Inc. 1

Sentron, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sentron”