Gresco Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gresco Products, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Gresco Products, Inc. has 7 FDA 510(k) cleared medical devices. Based in Stafford, US.
Historical record: 7 cleared submissions from 1985 to 1998. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Gresco Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gresco Products, Inc.
7 devices
Cleared
Jul 10, 1998
PRILANE
Dental
73d
Cleared
Oct 28, 1991
KAR-D-TEK
Dental
90d
Cleared
May 07, 1991
MET-ETCH
Dental
70d
Cleared
Mar 15, 1991
ENAMEL ETCHING GEL
Dental
17d
Cleared
Jun 01, 1990
CP-3 DENTAL POLISHING MATERIAL
Dental
31d
Cleared
Dec 27, 1985
GRESCO N.P. DENTAL ALLOY
Dental
45d
Cleared
Dec 23, 1985
CERAM-ETCH
Dental
41d