# Dmg Hamburg

- Location (FDA's records): Ayer, MA
- FDA decisions: 1 (1999–1999): 1 510(k) clearance
- Product codes: KLE (1)
- Predicates its devices cite: 1 (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
- Coltene/Whaledent, Inc.: 1 (https://510kreport.com/company/coltene-whaledent)

## Firms that cite its devices most
- Dmg USA, Inc.: 1 (https://510kreport.com/company/dmg-usa)

## Its most-cited devices
- K992879: Ecusit Composite Repair (1999), cited by 1

## Recent decisions
- K992879: Ecusit Composite Repair (Nov 9, 1999)

Source page: https://510kreport.com/company/dmg-hamburg