Gri Medical & Electronic Technology Co., Ltd. is one of 26038 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gri Medical & Electronic Technology Co., Ltd. - FDA 510(k) Cleared De...
Recent clearances: gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel Toddler, GRI STERILE AND NON-STERILE SURGICAL DRAPES AND SURGICAL EQUIPMENT COVERS, NON REINFORCED SURGICAL GOWNS, FILM REINFORCED SURGICAL GOWNS, FABRIC REINFORCED SURGICAL GOWNS
3
Total
3
Cleared
0
Denied
Gri Medical & Electronic Technology Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Swanee, US.
Historical record: 3 cleared submissions from 2011 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gri Medical & Electronic Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Resources Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Gri Medical & Electronic Technology Co., Ltd.
3 devices
Cleared
Nov 06, 2017
gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel...
General & Plastic Surgery
59d
Cleared
Dec 01, 2011
GRI STERILE AND NON-STERILE SURGICAL DRAPES AND SURGICAL EQUIPMENT COVERS
General Hospital
189d
Cleared
Feb 03, 2011
NON REINFORCED SURGICAL GOWNS, FILM REINFORCED SURGICAL GOWNS, FABRIC...
General Hospital
142d