# Anaxdent GmbH

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2002–2012): 2 510(k) clearances
- Product codes: EBG (1), EBF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K112044: Anaxblend Model 20XXX (Several), Anaxgum Model 25XXX (U), Mock-UP Direct Model 240XXX (U), Mock-UP Direct Flow Model 24A (Jan 26, 2012)
- K023079: New Outline (Oct 30, 2002)

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