FDA applicant

Genetic Laboratories Wound Care, Inc.

St. Paul, MN1 decision1993–19930 recalls

FDA records 1 decision for Genetic Laboratories Wound Care, Inc. (St. Paul, MN) in 1993: 1 510(k) clearance. All are in product code KGX (Tape And Bandage, Adhesive). 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 Genetic Laboratories Wound Care, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Genetic Laboratories Wound Care, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Genetic Laboratories Wound Care, 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 “Genetic”

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

Genetic Systems Corp. 12 Genetic Testing Institute 6 Genetic Laboratories, Inc. 4 Genetic Signatures Limited 1 Genetic 1

Genetic Laboratories Wound Care, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Genetic”