FDA applicant

Southside Biotechnology

Willoughby Hills, OH3 decisions1988–19900 recalls

FDA records 3 decisions for Southside Biotechnology (Willoughby Hills, OH) from 1988 to 1990: 3 510(k) clearances. Most are in product codes KGC (Tube, Gastro-Enterostomy) and KNT (Tubes, Gastrointestinal (And Accessories)). 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 Southside Biotechnology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Southside Biotechnology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Southside Biotechnology

Which product codes does it file in?

What has FDA decided for it lately?