Edward Weck, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Edward Weck, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WECK TROCAR, LM15(TM), CATALOG NUMBER - 523821, HEMOCLIP II
140
Total
140
Cleared
0
Denied
Edward Weck, Inc. has 140 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 140 cleared submissions from 1976 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Edward Weck, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Edward Weck, Inc.
140 devices
Cleared
Jun 29, 1992
WECK TROCAR
Obstetrics & Gynecology
213d
Cleared
Mar 23, 1992
LM15(TM), CATALOG NUMBER - 523821
General & Plastic Surgery
157d
Cleared
Jan 09, 1992
HEMOCLIP II
General & Plastic Surgery
254d
Cleared
Nov 29, 1991
PNEUMO-SEAL(TM)
General & Plastic Surgery
53d
Cleared
Jul 02, 1991
ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705
Obstetrics & Gynecology
102d
Cleared
Aug 06, 1990
HEM-O-LOK(TM)
General & Plastic Surgery
90d
Cleared
Aug 02, 1990
WECK ELECTROSURGICAL GENERATOR #174200
General & Plastic Surgery
77d
Cleared
Feb 15, 1990
BOWIE-DICK TEST CARD CATALOG NUMBER 008018
General Hospital
58d
Cleared
Aug 27, 1987
CORONARY ARTERY BYPASS GRAFT (CABG) MARKER
Cardiovascular
161d
Cleared
Jul 02, 1985
AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200
General & Plastic Surgery
97d
Cleared
Jun 07, 1985
WECK LX TM SKIN STAPLER
General & Plastic Surgery
71d
Cleared
Jan 23, 1985
HEMOCLIP X-20 AUTOMATIC HEMOCLIP LIGATING APPLIER
Microbiology
42d
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