# Altatec Biotechnologies

- Location (FDA's records): Potomac, MD
- FDA decisions: 4 (2000–2003): 4 510(k) clearances
- Product codes: DZE (3), NHA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (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
- Dentsply International, Inc.: 2 (https://510kreport.com/company/dentsply-international)
- Astra Tech, Inc.: 2 (https://510kreport.com/company/astra-tech)
- 3M Espe AG Dental Products: 1 (https://510kreport.com/company/3m-espe-ag-dental-products)
- Sirona Dental Systems GmbH: 1 (https://510kreport.com/company/sirona-dental-systems)

## Its most-cited devices
- K032448: Altatec Ceramic Abutment (2003), cited by 2
- K000100: Camlog Rootform Implant System (2000), cited by 2
- K000065: Camlog Cylinder Implant System (2000), cited by 1
- K000099: Camlog Screw Implant System (2000), cited by 1

## Recent decisions
- K032448: Altatec Ceramic Abutment (Aug 22, 2003)
- K000065: Camlog Cylinder Implant System (Jan 28, 2000)
- K000099: Camlog Screw Implant System (Jan 28, 2000)
- K000100: Camlog Rootform Implant System (Jan 28, 2000)

Source page: https://510kreport.com/company/altatec-biotechnologies