FDA applicant
Lifelong Meditech Private Limited
FDA records 2 decisions for Lifelong Meditech Private Limited (Gurgaon, IN) from 2021 to 2023: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 Lifelong Meditech Private Limited’s devices, and how often a recall has named them.
FDA decisions per year
1in 2023
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like Lifelong Meditech Private Limited’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