Valley Forge Scientific Corp. is one of 5539 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Valley Forge Scientific Corp. - FDA 510(k) Cleared Devices
Recent clearances: MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM, VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTS, STRYKER INTERVENTIONAL PAIN RF GENERATOR
27
Total
27
Cleared
0
Denied
Valley Forge Scientific Corp. has 27 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1980 to 2005.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Valley Forge Scientific Corp.
27 devices
Cleared
Mar 09, 2005
MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM
General & Plastic Surgery
23d
Cleared
Oct 22, 2004
VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED...
General & Plastic Surgery
28d
Cleared
Apr 01, 2004
STRYKER INTERVENTIONAL PAIN RF GENERATOR
Neurology
220d
Cleared
Nov 28, 2003
MALIS IRRIGATION MODULE 1000
General & Plastic Surgery
23d
Cleared
Aug 13, 1998
BI-DENT
Dental
90d
Cleared
Dec 19, 1997
VALLEY FORGE BIPOLAR BALL TIP ELECTRODE
General & Plastic Surgery
91d
Cleared
Aug 26, 1997
VALLEY FORGE BIPOLAR LOOP
Obstetrics & Gynecology
89d
Cleared
Jan 09, 1997
MINI-SYMM BIPOLAR COAGULATOR
General & Plastic Surgery
84d
Cleared
Mar 01, 1996
VALLEY FORGE BIPLOAR LOOP
General & Plastic Surgery
72d
Cleared
Dec 08, 1995
VFS - 300 BIPOLAR ELECTROSURGERY SYSTEM
General & Plastic Surgery
17d
Cleared
May 23, 1995
PRECISION BIPOLAR COAGULATOR
General & Plastic Surgery
26d
Cleared
Mar 11, 1993
AID, CARDIOPULMONARY RESUSCITATION
Anesthesiology
44d