# Hati Dental Ag.

- Location (FDA's records): Ridley Park, PA
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: DZE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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 that cite its devices most
- Thommen Medical AG: 3 (https://510kreport.com/company/thommen-medical)
- Paxmed International: 1 (https://510kreport.com/company/paxmed-international)
- Intra-Lock International: 1 (https://510kreport.com/company/intra-lock-international)

## Its most-cited devices
- K003045: HA-TI (Hand Titanium Screw) Implant (2001), cited by 5

## Recent decisions
- K003045: HA-TI (Hand Titanium Screw) Implant (Jul 12, 2001)

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