Medical Device Manufacturer · US , Kansas City , MO

Kay See Dental Mfg. Co. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999

Recent clearances: HYDRO-CAST BIS-ACRYL TEMPORARY CROWN AND BRIDGE MATERIAL, MODEL 98250, HYDRO-CAST SILICONE SOFT-LINER, MODEL 68400, HYDRO-CAST ACRYLIC VARNISH, MODEL 78125

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kay See Dental Mfg. Co. Dental ✕

5 devices

1-5 of 5

Cleared Jun 13, 2000

HYDRO-CAST BIS-ACRYL TEMPORARY CROWN AND BRIDGE MATERIAL, MODEL 98250

Cleared Sep 22, 1999

HYDRO-CAST SILICONE SOFT-LINER, MODEL 68400

Cleared Apr 29, 1999

HYDRO-CAST ACRYLIC VARNISH, MODEL 78125

Cleared Mar 03, 1999

HYDRO-CAST DENTAL ETCHING GEL, MODEL 60025

Cleared Feb 25, 1999

HYDRO-CAST VERSA-TEMP NON-EUGENOL PROVISIONAL CEMENT, MODEL 70010