FDA applicant
The South India Surgical Co. Pvt., Ltd.
FDA records 2 decisions for The South India Surgical Co. Pvt., Ltd. (India, IN) in 1989: 2 510(k) clearances. Most are in product codes LRW (Scissors, General, Surgical) and HCZ (Forceps, Surgical, Gynecological). 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 The South India Surgical Co. Pvt., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for The South India Surgical Co. Pvt., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like The South India Surgical Co. Pvt., 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