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

Baui Biotech Co., Ltd.

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

Total Devices5
Categories2
Latest FDA decision2024-10-17
TypeNumberDevice NameCodeDateActions
510(k) K242899 NOVA Minimally Invasive SystemNKB2024-10-17 View
510(k) K191353 COMET Lumbar Interbody Fusion CageMAX2020-04-14 View
510(k) K191494 Facilis™ Spinal SystemNKB2019-08-12 View
510(k) K182416 NOVA Minimally Invasive SystemNKB2019-06-11 View
510(k) K161231 Facilis™ Spinal SystemNKB2017-01-23 View