Omnigrace (Thailand) , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omnigrace (Thailand) , Ltd. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Omnigrace (Thailand) , Ltd. has 12 FDA 510(k) cleared general hospital devices. Based in North Canton, US.
Historical record: 12 cleared submissions from 1998 to 2001.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omnigrace (Thailand) , Ltd.
12 devices
Cleared
Oct 12, 2001
OMNI GRACE LATEX EXAMINATION GLOVE, POWDER FREE, POLYMER COATED WITH PROTEIN...
General Hospital
77d
Cleared
Oct 16, 2000
OMNI GRACE LATEX EXAMINATION GLOVE, POWDERED, WITH PROTEIN CLAIM (200...
General Hospital
27d
Cleared
Nov 19, 1999
OMNI GRACE LATEX EXAMINATION GLOVE, POWDERED, WITH PROTEIN CLAIM (100...
General Hospital
36d
Cleared
May 13, 1999
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE,WHITE
General Hospital
71d
Cleared
May 13, 1999
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED PURPLE
General Hospital
71d
Cleared
May 05, 1999
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE, PURPLE
General Hospital
63d
Cleared
May 04, 1999
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED WHITE
General Hospital
62d
Cleared
May 04, 1999
OMNI GRACE LATEX EXAMINATION GLOVE, POWDER-FREE, POLYMER COATED WITH PROTEIN...
General Hospital
62d
Cleared
Nov 30, 1998
OMNIGRACE LATEX EXAMINATION GLOVE, POWDER-FREE, WITH PROTEIN CLAIM
General Hospital
118d
Cleared
Sep 02, 1998
OMNI PRO LATEX SURGICAL GLOVE, POWDERED
General Hospital
37d
Cleared
Mar 13, 1998
OMNI FLEX NITRILE EXAMINATION GLOVE, POWDER-FREE
General Hospital
38d
Cleared
Mar 13, 1998
OMNI TOUCH NITRILE EXAMINATION GLOVE, POWDERED
General Hospital
38d