FDA applicant

Blue & Red Corp.

Merrick, NY1 decision1990–19900 recalls

FDA records 1 decision for Blue & Red Corp. (Merrick, NY) in 1990: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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 Blue & Red Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Blue & Red Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Blue & Red Corp.’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 “Blue”

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

Blue Belt Technologies, Inc. 22 Blue Sky Bio, LLC 21 Blue Ridge Media Co. 11 Blue Ortho 9 Blue Sky Medical Group Incorporated 4 Blue Planet Industries, Inc. 3 Blue Torch Medical Technologies 2 Blue Sail Medical Co.,Ltd 2 Blue X Imaging Srl 2 Blue Spark Technologies, Inc. 2 Blue Focus 1 Blue Gem Sunglasses, Inc. 1

Blue & Red Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Blue”