Valley Forge Scientific Corp.

FDA Regulatory Profile

Valley Forge Scientific Corp. has 0 FDA recalls, 0 inspections, 27 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Valley Forge Scientific Corp." and its spelling variant "Valley Forge Scientific".

Latest 510(k)
Mar 9, 2005

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances27Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) clearances

27 510(k) clearances from Jun 20, 1980 to Mar 9, 2005. Showing the 20 most recent. View all 27 510(k) clearances

K-NumberDeviceDate
K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMMar 9, 2005
K042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSOct 22, 2004
K032601STRYKER INTERVENTIONAL PAIN RF GENERATORApr 1, 2004
K033499MALIS IRRIGATION MODULE 1000Nov 28, 2003
K982229BI-DENTAug 13, 1998
K973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODEDec 19, 1997
K971986VALLEY FORGE BIPOLAR LOOPAug 26, 1997
K964143MINI-SYMM BIPOLAR COAGULATORJan 9, 1997
K955764VALLEY FORGE BIPLOAR LOOPMar 1, 1996
K955346VFS - 300 BIPOLAR ELECTROSURGERY SYSTEMDec 8, 1995
K951985PRECISION BIPOLAR COAGULATORMay 23, 1995
K930429AID, CARDIOPULMONARY RESUSCITATIONMar 11, 1993
K923928BIPOLAR COAGULATOR/IRRIAGATION SYSTEMJan 22, 1993
K924188BI-TECH I BIPOLAR COAGULATOR/CUTTING SYSTEMDec 10, 1992
K910510VALLEY FORGE BIPOLAR PEN OR FORCEPSApr 22, 1991
K896541MALIS BIPOLAR ELECTROSURGICAL SYSTEM CMC-IIIJan 29, 1990
K890648MALIS BIPOLAR CORD/IRRIGATION TUBING SETMar 3, 1989
K890309MALIS SURGICAL STOOLFeb 14, 1989
K874845MALIS SURGICAL LOUPESDec 23, 1987
K861822MALIS SURGICAL MESH FOR SKULL /SPINAL COLUMN REPAIJul 11, 1986

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.