Medical Device Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Device Technologies, Inc. - FDA 510(k) Cleared Devices
46
Total
46
Cleared
0
Denied
Medical Device Technologies, Inc. has 46 FDA 510(k) cleared medical devices. Based in Gainsville, US.
Historical record: 46 cleared submissions from 1992 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medical Device Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Device Technologies, Inc.
46 devices
Cleared
Aug 27, 2010
BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT
Gastroenterology & Urology
57d
Cleared
Jan 26, 2006
INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
General & Plastic Surgery
38d
Cleared
Aug 30, 2005
INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
General & Plastic Surgery
90d
Cleared
May 26, 2005
CANALIZER HYDROPHILIC GUIDE WIRE
Cardiovascular
50d
Cleared
Feb 11, 2005
INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE
Gastroenterology & Urology
53d
Cleared
Sep 30, 2004
V-CORE FULL CORE BREAST BIOPSY INSTRUMENT
Gastroenterology & Urology
17d
Cleared
May 03, 2004
FIBREX CATHETER PATENCY DEVICE
General Hospital
74d
Cleared
Aug 13, 2003
PBN GUIDEWIRES
Cardiovascular
99d
Cleared
May 31, 2002
EN-SNARE ENDOVASCULAR SNARE AND CATHETER
Cardiovascular
15d
Cleared
Sep 05, 2001
MICROCRUISER PLUS INTRODUCER SET
Cardiovascular
89d
Cleared
Oct 30, 2000
PBN FALLOPIAN TUBE CATHETER SYSTEM
Obstetrics & Gynecology
249d
Cleared
Sep 11, 2000
GOLDEN-RULE SCALING CATHETER
Cardiovascular
34d
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