Omnigrace , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omnigrace , Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Omnigrace , Ltd. has 8 FDA 510(k) cleared medical devices. Based in Canton, US.
Historical record: 8 cleared submissions from 1997 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Omnigrace , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omnigrace , Ltd.
8 devices
Cleared
Jan 31, 2000
OMNI GRACE NITRILE, BLUE, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED
General Hospital
46d
Cleared
Nov 19, 1999
OMNIGRACE LATEX EXAMINATION GLOVE, POWDER-FREE
General Hospital
38d
Cleared
Nov 09, 1999
OMNI GRACE NITRILE, GREEN, EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED
General Hospital
60d
Cleared
Aug 05, 1999
PATIENT EXAMINATION GLOVES, NITRILE POWDER FREE, TURQUOISE,NON-STERILE.
General Hospital
69d
Cleared
Aug 05, 1999
PATIENT EXAMINATION GLOVE, NITRILE, POWDERED, TURQUOISE, NON-STERILE
General Hospital
69d
Cleared
Dec 11, 1998
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE, BLUE
General Hospital
50d
Cleared
Dec 07, 1998
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED, BLUE
General Hospital
46d
Cleared
Nov 06, 1997
OMNI F.T. LATEX EXAMINATION GLOVE, POWDERED
General Hospital
77d