# Dentmate Technology Co., Ltd.

- Location (FDA's records): New Taipei, TW
- FDA decisions: 4 (2008–2022): 4 510(k) clearances
- Product codes: EBZ (4)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Premium Plus International Limited: 1 (https://510kreport.com/company/premium-plus-international)
- Premium Plus (Dongguan) Limited: 1 (https://510kreport.com/company/premium-plus-dongguan)

## Its most-cited devices
- K131042: LEDEX (2013), cited by 1
- K082408: Ledex, Model: WL-070 (2008), cited by 1
- K221194: LEDEX (2022), cited by 1

## Recent decisions
- K221194: LEDEX (Sep 16, 2022)
- K163605: Ledex WL070+ (Jan 19, 2017)
- K131042: LEDEX (Oct 3, 2013)
- K082408: Ledex, Model: WL-070 (Dec 3, 2008)

Source page: https://510kreport.com/company/dentmate-technology