FDA applicant
Eschmann Bros. & Walsh, Ltd.
FDA records 3 decisions for Eschmann Bros. & Walsh, Ltd. (Sussex Bn15 8tj, GB) from 1978 to 1987: 3 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and HHW (Pessary, Vaginal). 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 Eschmann Bros. & Walsh, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Eschmann Bros. & Walsh, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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