FDA applicant
American Cyanamid Co.
FDA records 7 decisions for American Cyanamid Co. (Danbury, CT) from 1983 to 1993: 7 510(k) clearances. Most are in product codes GDW (Staple, Implantable) 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
How often FDA has decided American Cyanamid Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for American Cyanamid Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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