FDA applicant

Lincoln Laboratories, Inc.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Lincoln Laboratories, Inc. (Mchenry, IL) in 1976: 1 510(k) clearance. 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 Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lincoln Laboratories, 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 “Lincoln”

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

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

Lincoln Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lincoln”