Medical Device Manufacturer · US , Tempe , AZ

Medi-Globe Corporation - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006
7
Total
7
Cleared
0
Denied

Medi-Globe Corporation has 7 FDA 510(k) cleared medical devices. Based in Tempe, US.

Historical record: 7 cleared submissions from 2006 to 2016. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Medi-Globe Corporation Filter by specialty or product code using the sidebar.

7 devices
1–7 of 7
EasyPass Guidewire
K153264 · OCY Endoscopic Guidewire, Gastroenterology-urology · Gastroenterology & Urology
May 2016 189d
PolyCatch Retrieval Device
K142258 · FDI Snare, Flexible · Gastroenterology & Urology
Sep 2014 47d
SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM
K133763 · FCG Biopsy Needle · Gastroenterology & Urology
May 2014 155d
MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM
K091257 · FCG Biopsy Needle · Gastroenterology & Urology
May 2009 9d
SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025
K083802 · FCG Biopsy Needle · Gastroenterology & Urology
Mar 2009 88d
SONOTIP II ULTRASOUND NEEDLE SYSTEM
K070129 · FCG Biopsy Needle · Gastroenterology & Urology
Jan 2007 15d
MEDI-GLOBE ROTA-CUT SPHINCTEROTOME
K061684 · KNS Unit, Electrosurgical, Endoscopic (with Or Without Accessories) · Gastroenterology & Urology
Jun 2006 12d
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