# Phoenix Dental, Inc.

- Location (FDA's records): Fenton, MI
- FDA decisions: 5 (1994–2012): 5 510(k) clearances
- Product codes: DZE (2), EJK (1), LFC (1), LBH (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 10 (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
- Kuraray Medical, Inc.: 1 (https://510kreport.com/company/kuraray-medical)
- Sunstar Butler: 1 (https://510kreport.com/company/sunstar-butler)
- Del Pharmaceuticals, Inc.: 1 (https://510kreport.com/company/del-pharmaceuticals)

## Firms that cite its devices most
- Bisco, Inc.: 3 (https://510kreport.com/company/bisco)
- Centrix, Inc.: 2 (https://510kreport.com/company/centrix)
- Swiss Dental Center: 2 (https://510kreport.com/company/swiss-dental-center)
- Inter-Med, Inc.: 1 (https://510kreport.com/company/inter-med)
- Kuraray Noritake Dental, Inc.: 1 (https://510kreport.com/company/kuraray-noritake-dental)
- Remedent NV: 1 (https://510kreport.com/company/remedent)

## Its most-cited devices
- K983477: Super Seal (1998), cited by 5
- K120109: Super Seal Tooth Desensitizer (2012), cited by 3
- K926101: Phoenix Opti-Max Dent Impl W/Plas-Spray Tita/Hydro (1994), cited by 1
- K926102: Phoenix Opti-Max Dent Implant W/Plasma-Spray Titan (1994), cited by 1

## Recent decisions
- K120109: Super Seal Tooth Desensitizer (Mar 7, 2012)
- K102821: Discovred (Mar 11, 2011)
- K983477: Super Seal (Dec 22, 1998)
- K926101: Phoenix Opti-Max Dent Impl W/Plas-Spray Tita/Hydro (Jun 23, 1994)
- K926102: Phoenix Opti-Max Dent Implant W/Plasma-Spray Titan (Jun 22, 1994)

Source page: https://510kreport.com/company/phoenix-dental