FDA applicant

Akers Research Corp.

Thorofare, NJ3 decisions1992–19920 recalls

FDA records 3 decisions for Akers Research Corp. (Thorofare, NJ) in 1992: 3 510(k) clearances. Most are in product codes LJO (Antigen, Iha, Cytomegalovirus) and DHR (System, Test, Rheumatoid Factor). 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, immunology panel, where it files most

How often FDA has decided Akers Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Akers Research Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Akers Research Corp.’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 “Akers”

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

Akers Biosciences, Inc. 5 Akers Laboratories, Inc. 3 Akers Medical Technologies 1

Akers Research Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Akers”