FDA applicant

Gbf Medical Group

Greensboro, NC1 decision1994–19940 recalls

FDA records 1 decision for Gbf Medical Group (Greensboro, NC) in 1994: 1 510(k) clearance. All are in product code KDW (Container, Specimen Mailer And Storage…). 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, pathology panel, where it files most

How often FDA has decided Gbf Medical Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gbf Medical Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Gbf Medical Group

Which product codes does it file in?

What has FDA decided for it lately?