FDA applicant

Wright Laboratories, Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Wright Laboratories, Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code JQW (Station, Pipetting And Diluting, For Clinical…). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Wright Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Wright Laboratories, 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 “Wright”

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

Wright Medical Corp. 6 Wright Linear Pump, Inc. 6 Wright Medical Technology, Inc. (Stryker) 5 Wright Industries 1 Wright Therapy Products, Inc. 1 Wright Medical Technology 1 Wright Health Group, Ltd. 1

Wright Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Wright”