Medical Device Manufacturer · US , Fort Lauderdale , FL

Orbus Medical Technologies - FDA 510(k) Cleared Devices

8 submissions · 0 cleared · Since 2001

8

Total

0

Cleared

0

Denied

Orbus Medical Technologies has 0 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.

Historical record: 0 cleared submissions from 2001 to 2004. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Orbus Medical Technologies Filter by specialty or product code using the sidebar.

Orbus Medical Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Orbus Medical Technologies

8 devices

1-8 of 8

Cleared Jun 24, 2004

LIFESTENT LP SDS BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 31d

Cleared May 10, 2004

MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 19d

Cleared Mar 16, 2004

LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 14d

Cleared Oct 30, 2003

LIFESTENT SDS BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 27d

Cleared Apr 14, 2003

LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 193d

Cleared Mar 10, 2003

LIFESTENT BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 172d

Cleared Feb 11, 2003

LIFESTENT LP SDS BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 134d

Cleared Jul 31, 2001

R STENT BILIARY ENDOPROSTHESIS

Gastroenterology & Urology · 200d