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.

Filmecc Co., Ltd.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories1
Latest Approval2023-03-09
TypeNumberDevice NameCodeDate
510(k) K223432 Vassallo GT 018 Hybrid DQX 2023-03-09 View
510(k) K222631 VASSALLO GT EXT DQX 2022-10-26 View
510(k) K213949 VASSALLO GT 018 Floppy DQX 2022-06-30 View
510(k) K203529 VASSALLO GT Hybrid DQX 2021-05-04 View
510(k) K203533 VASSALLO GT DQX 2021-04-21 View