FDA applicant

Blue Planet Industries, Inc.

Plymouth, MN3 decisions1994–19940 recalls

FDA records 3 decisions for Blue Planet Industries, Inc. (Plymouth, MN) in 1994: 3 510(k) clearances. Most are in product codes FEB (Accessories, Cleaning, For Endoscope) and HIF (Insufflator, Laparoscopic). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Blue Planet Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Blue Planet Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Blue Planet Industries, 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 “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 Torch Medical Technologies 2 Blue Sail Medical Co.,Ltd 2 Blue X Imaging Srl 2 Blue Spark Technologies, Inc. 2 Blue & Red Corp. 1 Blue Focus 1 Blue Gem Sunglasses, Inc. 1

Blue Planet Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Blue”