Instrumed International, Inc. is one of 503 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Instrumed International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054, INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXX, INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL
7
Total
7
Cleared
0
Denied
Instrumed International, Inc. has 7 FDA 510(k) cleared medical devices. Based in Tuningen, B.W., DE.
Historical record: 7 cleared submissions from 2004 to 2010.
Browse the FDA 510(k) cleared devices submitted by Instrumed International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Instrumed International, Inc.
7 devices
Cleared
Aug 31, 2010
INSTRUMED VESSEL DILATORS, MODEL 65-7XX,65-9XXX,66-1XXX,65-7048-65-7054
Cardiovascular
189d
Cleared
Apr 29, 2010
INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXX
Obstetrics & Gynecology
65d
Cleared
Dec 03, 2009
INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL
Obstetrics & Gynecology
79d
Cleared
Oct 26, 2009
INSTRUMED VASCULAR CLAMPS
Cardiovascular
68d
Cleared
Aug 08, 2008
INSTRUMED RONGEUR
Neurology
57d
Cleared
Aug 02, 2007
INSTRUMED RETRACTORS
Neurology
34d
Cleared
Apr 16, 2004
INSTRUMED LAPAROSCOPE AND ACCESSORIES
General & Plastic Surgery
14d