# Friatec AG

- Location (FDA's records): Potomac, MD
- FDA decisions: 6 (1998–1998): 6 510(k) clearances
- Product codes: DZE (5), JEY (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- Implant Innovations International, Inc.: 1 (https://510kreport.com/company/implant-innovations-international)

## Firms that cite its devices most
- Sulzer Dental, Inc.: 2 (https://510kreport.com/company/sulzer-dental)
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)
- Dentsply International, Inc.: 1 (https://510kreport.com/company/dentsply-international)
- Friadent GmbH: 1 (https://510kreport.com/company/friadent)

## Its most-cited devices
- K980630: Frialit-2 Corabase (1998), cited by 3
- K974628: Frialit-2 Protect Abutment (1998), cited by 1
- K974358: Frialit -2 Screw (1998), cited by 1

## Recent decisions
- K982576: Frialit-2 Aurobase Model Numbers 45-2446, 45-2456, 45-2466, 45-2476 (Oct 22, 1998)
- K980630: Frialit-2 Corabase (Sep 4, 1998)
- K973924: Frios Boneshield (May 7, 1998)
- K974628: Frialit-2 Protect Abutment (Mar 11, 1998)
- K974359: Frialit-2 Cylinder (Feb 10, 1998)
- K974358: Frialit -2 Screw (Feb 10, 1998)

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