Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Timpel S.A.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories1
Latest Approval2025-09-10
TypeNumberDevice NameCodeDate
510(k) K250464 Enlight 2100 (TPL-E2103-0) QEB 2025-09-10 View
510(k) K222897 Enlight 2100 QEB 2023-03-07 View
510(k) K211135 Enlight 2100 QEB 2022-01-06 View