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.

Megagen Co., Ltd.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K110955 ANYRIDGE INTERNAL IMPLANT SYSTEMDZE2011-11-22 View
510(k) K101890 BALL ABUTMENT SYSTEMNHA2011-02-03 View
510(k) K073058 RESCUE INTERNAL IMPLANT SYSTEMDZE2008-04-11 View
510(k) K070562 EZ PLUS IMPLANT SYSTEMNHA2007-05-18 View
510(k) K063216 RESCUE INTERNAL IMPLANT SYSTEMDZE2007-04-02 View
510(k) K053353 RESCUE IMPLANT SYSTEMDZE2006-04-19 View
510(k) K053354 INTERMEZZO PLUS FIXTUREDZE2006-04-13 View
510(k) K052369 EXFEEL IMPLANT SYSTEMDZE2006-01-10 View
510(k) K051018 INTERMEZZO IMPLANT SYSTEMSDZE2005-09-02 View
↑