Genesis Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Genesis Industries, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Genesis Industries, Inc. has 17 FDA 510(k) cleared dental devices. Based in Walker, US.
Historical record: 17 cleared submissions from 1983 to 2000.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Genesis Industries, Inc.
17 devices
Cleared
Feb 18, 2000
ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP...
Obstetrics & Gynecology
53d
Cleared
Feb 10, 1997
EVERT-IT
Obstetrics & Gynecology
206d
Cleared
Apr 04, 1988
NOVO VIVO MODEL #17140 AND #17135
General & Plastic Surgery
68d
Cleared
Feb 16, 1988
NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP
General & Plastic Surgery
20d
Cleared
Jan 03, 1984
SATIN CAST ECONOCAST
Dental
103d
Cleared
Jan 03, 1984
C & B 40 PENTRO C & B40
Dental
103d
Cleared
Dec 29, 1983
C & B 45
Dental
98d
Cleared
Dec 29, 1983
C & B 61 PENTRON C & B61
Dental
98d
Cleared
Dec 26, 1983
SUPRA AP CHOICE 83
Dental
95d
Cleared
Dec 22, 1983
RX IV PENTRON IV
Dental
91d
Cleared
Dec 20, 1983
C & B57 PENTRON C & B57
Dental
89d
Cleared
Nov 28, 1983
NATURELLE-LITE
Dental
67d