FDA applicant

The Tulip Mfg. Co.

Mesa, AZ24 decisions1995–19960 recalls

FDA records 24 decisions for The Tulip Mfg. Co. (Mesa, AZ) from 1995 to 1996: 24 510(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 The Tulip Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Tulip Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Tulip Mfg. Co.

Which product codes does it file in?

What has FDA decided for it lately?