# Dentamerica

- Location (FDA's records): Industry, CA
- FDA decisions: 4 (1996–2010): 4 510(k) clearances
- Product codes: ELC (1), EKX (1), EHD (1), EBZ (1)
- Predicates its devices cite: 5 (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
- Nsk Nakanishi, Inc.: 1 (https://510kreport.com/company/nsk-nakanishi)
- J. Morita USA, Inc.: 1 (https://510kreport.com/company/j-morita-usa)
- Visiodent SA: 1 (https://510kreport.com/company/visiodent)
- Afp Imaging Corp.: 1 (https://510kreport.com/company/afp-imaging)
- Gendex Corp.: 1 (https://510kreport.com/company/gendex)

## Firms that cite its devices most
- Saeyang Microtech Co., Ltd.: 1 (https://510kreport.com/company/saeyang-microtech)

## Its most-cited devices
- K092833: Endomax Cordless Endodontic Handpiece (2010), cited by 1

## Recent decisions
- K092833: Endomax Cordless Endodontic Handpiece (Jan 7, 2010)
- K060640: Digirex Digital Dental Radiography System (Apr 24, 2006)
- K954820: Scalex 800 (Jan 18, 1996)
- K955759: LITEX 680 (Jan 2, 1996)

Source page: https://510kreport.com/company/dentamerica