Medi-Globe Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medi-Globe Corp. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Medi-Globe Corp. has 17 FDA 510(k) cleared gastroenterology & urology devices. Based in Irvine, US.
Historical record: 17 cleared submissions from 1990 to 2006.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medi-Globe Corp.
18 devices
Cleared
Jul 03, 2006
INJECTRA INJECTION NEEDLE
Gastroenterology & Urology
62d
Cleared
Jun 16, 2005
SONOTIP II ULTRASOUND NEEDLE SYSTEM
Gastroenterology & Urology
31d
Cleared
Nov 17, 2003
STONE EXTRACTOR BALLOON CATHETER
Gastroenterology & Urology
936d
Cleared
Jan 21, 2003
EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830
Gastroenterology & Urology
683d
Cleared
Jan 18, 2002
BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)
Gastroenterology & Urology
326d
Cleared
Mar 31, 1999
MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM
Gastroenterology & Urology
68d
Cleared
Apr 04, 1996
GIP/MEID-GLOBE HOT BIOPSY FORCEPS
Gastroenterology & Urology
262d
Cleared
Feb 29, 1996
GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES
Gastroenterology & Urology
85d
Cleared
Sep 01, 1995
GIP/MEDI-GLOBE ERCP CATHETERS
Gastroenterology & Urology
17d
Cleared
Jun 30, 1995
GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES
Gastroenterology & Urology
434d
Cleared
May 26, 1995
GIP/MEDI-GLOBE PAPILLOTOME
Gastroenterology & Urology
304d
Cleared
May 26, 1995
GIP/MEDI-GLOBE POLYPECTOMY SNARES
Gastroenterology & Urology
287d