FDA applicant
Shangrila Latex Industries Pvt., Ltd.
FDA records 3 decisions for Shangrila Latex Industries Pvt., Ltd. (Bombay 400 026, IN) from 1990 to 1996: 3 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and KGO (Surgeon'S Gloves). 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 Shangrila Latex Industries Pvt., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Shangrila Latex Industries Pvt., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Shangrila Latex Industries 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