Gainor Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gainor Medical - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Gainor Medical has 11 FDA 510(k) cleared general & plastic surgery devices. Based in US.
Historical record: 11 cleared submissions from 1984 to 1987.
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 - Gainor Medical
11 devices
Cleared
Jan 29, 1987
BLOOD LANCET
General & Plastic Surgery
748d
Cleared
Feb 21, 1985
ULSTER SCIENTIFIC, INC. AUTOLET LANCETS/GAINOR MED
General & Plastic Surgery
38d
Cleared
Nov 30, 1984
GAINOR MEDICAL FLOWMAX NEEDLES
General Hospital
24d
Cleared
Nov 30, 1984
GAINOR MEDICAL SYRINGE
General Hospital
24d
Cleared
Oct 31, 1984
SKIN CLOSURE
General & Plastic Surgery
240d
Cleared
Oct 31, 1984
ZINC OXIDE TAPE
General & Plastic Surgery
240d
Cleared
Oct 31, 1984
FIRST AID BANDAGE
General & Plastic Surgery
240d
Cleared
Aug 17, 1984
MICROPOROUS HYPOALLERGENIC
General & Plastic Surgery
165d
Cleared
Aug 17, 1984
CLOTH-HYPOALLERGENIC
General & Plastic Surgery
165d
Cleared
Aug 17, 1984
CLEAR PLASTIC-HYPOALLERGENIC
General & Plastic Surgery
165d
Cleared
Aug 14, 1984
CLEAR POROUS PLASTIC-HYPOALLERGENIC
Hematology
39d