Orbus Medical Technologies
Orbus Medical Technologies holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2004.
Top product codes for Orbus Medical Technologies
Recent clearances by Orbus Medical Technologies
- K041370 — LIFESTENT LP SDS BILIARY ENDOPROSTHESIS
- K041032 — MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS
- K040550 — LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS
- K033212 — LIFESTENT SDS BILIARY ENDOPROSTHESIS
- K023308 — LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS
- K023121 — LIFESTENT BILIARY ENDOPROSTHESIS
- K023248 — LIFESTENT LP SDS BILIARY ENDOPROSTHESIS
- K010107 — R STENT BILIARY ENDOPROSTHESIS
Data sourced from openFDA. This site is unofficial and independent of the FDA.