Kay See Dental Mfg. Co. is one of 10897 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kay See Dental Mfg. Co. - FDA 510(k) Cleared Devices
Recent clearances: HYDRO-CAST SILICONE SOFT-LINER, MODEL 68400, HYDRO-CAST ACRYLIC VARNISH, MODEL 78125, HYDRO-CAST DENTAL ETCHING GEL, MODEL 60025
5
Total
5
Cleared
0
Denied
Kay See Dental Mfg. Co. has 5 FDA 510(k) cleared medical devices. Based in Kansas City, US.
Historical record: 5 cleared submissions from 1999 to 2000. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Kay See Dental Mfg. Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kay See Dental Mfg. Co.
5 devices
Cleared
Jun 13, 2000
HYDRO-CAST BIS-ACRYL TEMPORARY CROWN AND BRIDGE MATERIAL, MODEL 98250
Dental
49d
Cleared
Sep 22, 1999
HYDRO-CAST SILICONE SOFT-LINER, MODEL 68400
Dental
49d
Cleared
Apr 29, 1999
HYDRO-CAST ACRYLIC VARNISH, MODEL 78125
Dental
22d
Cleared
Mar 03, 1999
HYDRO-CAST DENTAL ETCHING GEL, MODEL 60025
Dental
30d
Cleared
Feb 25, 1999
HYDRO-CAST VERSA-TEMP NON-EUGENOL PROVISIONAL CEMENT, MODEL 70010
Dental
37d