FDA applicant
American Hydro-Surgical Instruments, Inc.
FDA records 18 decisions for American Hydro-Surgical Instruments, Inc. (Delray Beach, FL) from 1993 to 1995: 18 510(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
How often FDA has decided American Hydro-Surgical Instruments, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for American Hydro-Surgical Instruments, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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