FDA applicant

Jensen Industries, Inc.

North Haven, CT17 decisions1998–20190 recalls

FDA records 17 decisions for Jensen Industries, Inc. (North Haven, CT) from 1998 to 2019: 17 510(k) clearances. Most are in product codes EIH (Powder, Porcelain) and EJT (Alloy, Gold-Based Noble Metal). Its devices cite 13 predicates, 6 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, dental panel, where it files most

How often FDA has decided Jensen Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2007high 2 (2011) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Jensen”

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

Jensen Int'L, Inc. 1 Jensen Union Ent. Co., Ltd. 1

Jensen Industries, Inc.

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 “Jensen”