FDA applicant

Derma Care Plus Products, LLC

Green Bay, WI2 decisions2007–20110 recalls

FDA records 2 decisions for Derma Care Plus Products, LLC (Green Bay, WI) from 2007 to 2011: 2 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and LZA (Polymer Patient Examination Glove). 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 Derma Care Plus Products, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Derma Care Plus Products, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Derma”

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

Derma Sciences, Inc. 22 Derma Media Lab., Inc. 18 Derma-Lase Co. 5 Derma Sciences Canada, Inc. 3 Derma-Lock Medical Corp. 2 Derma-Safe Co. 2

Derma Care Plus Products, LLC

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Derma”