# Kay See Dental Mfg. Co.

- Location (FDA's records): Kansas City, MO
- FDA decisions: 5 (1999–2000): 5 510(k) clearances
- Product codes: EBG (1), EBI (1), EBC (1), EIA (1), EMA (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ortho Source: 1 (https://510kreport.com/company/ortho-source)
- Kulzer, Inc.: 1 (https://510kreport.com/company/kulzer)
- Scientific Pharmaceuticals, Inc.: 1 (https://510kreport.com/company/scientific-pharmaceuticals)

## Firms that cite its devices most
- Meta Biomed Co., Ltd.: 1 (https://510kreport.com/company/meta-biomed)

## Its most-cited devices
- K001309: Hydro-Cast Bis-Acryl Temporary Crown and Bridge Material, Model 98250 (2000), cited by 1

## Recent decisions
- K001309: Hydro-Cast Bis-Acryl Temporary Crown and Bridge Material, Model 98250 (Jun 13, 2000)
- K992609: Hydro-Cast Silicone Soft-Liner, Model 68400 (Sep 22, 1999)
- K991161: Hydro-Cast Acrylic Varnish, Model 78125 (Apr 29, 1999)
- K990306: Hydro-Cast Dental Etching Gel, Model 60025 (Mar 3, 1999)
- K990155: Hydro-Cast Versa-Temp Non-Eugenol Provisional Cement, Model 70010 (Feb 25, 1999)

Source page: https://510kreport.com/company/kay-see-dental-mfg