FDA applicant
Veol Medical Technologies Pvt, Ltd.
FDA records 2 decisions for Veol Medical Technologies Pvt, Ltd. (Navi Mumbai, IN) from 2024 to 2025: 2 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and FBK (Endoscopic Injection Needle…). Its devices cite 2 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 Veol Medical Technologies Pvt, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Veol Medical Technologies 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