FDA applicant

Lincoln Diagnostics, Inc.

Decatur, IL2 decisions1994–19960 recalls

FDA records 2 decisions for Lincoln Diagnostics, Inc. (Decatur, IL) from 1994 to 1996: 2 510(k) clearances. All are in product code SCL (Allergen And Vaccine Delivery Needles). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Lincoln Diagnostics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lincoln”

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

Lincoln Mills, Inc. 2 Lincoln Park Dental Laboratory 1 Lincoln Laboratories, Inc. 1

Lincoln Diagnostics, Inc.

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?

Other applicant names beginning “Lincoln”