Not currently registered with FDA under this name
Kay See Dental Mfg. Co.
Kansas City, MO, United States. Named as applicant on 5 dental 510(k) clearances between 1999 and 2000. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51999–2000
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Kay See Dental Mfg. Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 13 Jun 2000 | K001309 | HYDRO-CAST BIS-ACRYL TEMPORARY CROWN AND BRIDGE MATERIAL, MODEL 98250 | EBG Resin Temporary Crown and Bridge |
| 22 Sep 1999 | K992609 | HYDRO-CAST SILICONE SOFT-LINER, MODEL 68400 | EBI Rebasing Repairing Relining Denture Resin |
| 29 Apr 1999 | K991161 | HYDRO-CAST ACRYLIC VARNISH, MODEL 78125 | EIA Operative Dental Unit |
| 3 Mar 1999 | K990306 | HYDRO-CAST DENTAL ETCHING GEL, MODEL 60025 | EBC Pit and Fissure Sealant and Conditioner |
| 25 Feb 1999 | K990155 | HYDRO-CAST VERSA-TEMP NON-EUGENOL PROVISIONAL CEMENT, MODEL 70010 | EMA Dental Cement |
Some of these clearances are listed with FDA today by another company: Dentsply Sirona, Inc. (1), indigodental GmbH (1), Sterngold (1), DMG Chemisch-Pharmazeutische Fabrik GmbH (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.