FDA applicant

Springfield Surgical Instruments

Brimfield, MA8 decisions1993–19950 recalls

FDA records 8 decisions for Springfield Surgical Instruments (Brimfield, MA) from 1993 to 1995: 8 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 Springfield Surgical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Springfield Surgical Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Springfield Surgical Instruments

Which product codes does it file in?

What has FDA decided for it lately?