FDA applicant
Matsutani Seisakusho Co., Ltd.
FDA records 1 decision for Matsutani Seisakusho Co., Ltd. (Mahwah, NJ) in 1993: 1 510(k) clearance. All are in product code GDT (Staple, Removable (Skin)). 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 Matsutani Seisakusho Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Matsutani Seisakusho Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Matsutani Seisakusho Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report