Friadent GmbH
Friadent GmbH holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2004.
Top product codes for Friadent GmbH
Recent clearances by Friadent GmbH
- K040170 — FRIADENT PLUS DENTAL IMPLANT SYSTEMS
- K041509 — ANKYLOS DENTAL IMPLANT SYSTEM
- K040946 — ANKYLOS DENTAL IMPLANT SYSTEM
- K032302 — XIVE TG ABUTMENTS
- K031674 — MODIFICATION TO FRIALIT-2 DENTAL IMPLANT SYSTEM
- K032158 — XIVE DENTAL IMPLANT SYSTEM MULTIPLE
- K032284 — XIVE TG DENTAL IMPLANT SYSTEM
- K024004 — XIVE TRANSGINGIVAL DENTAL IMPLANT SYSTEM
- K023799 — FRIOS ALGIPORE
- K021318 — XIVE DENTAL IMPLANT SYSTEM
- K013067 — FRIALOC DENTAL IMPLANT SYSTEM
- K013867 — XIVE DENTAL IMPLANT SYSTEM
- K013438 — FRIALIT-2 ESTHETICBASE ABUTMENT
- K994174 — FRIALIT-2 MH-2 ABUTMENT
- K994376 — FRIALIT-2 3.4MM STEEPED CYLINDER IMPLANT WITH FRIOS TPS COATING; FRIALIT-2 3.4MM STEEPED CYLINDER IMPLANT WITH FRIOS HA
- K994298 — FRIOS MICROSAW
- K993560 — FRIALIT-2 BONE PROFILER
- K993095 — FRIALIT-2 SELECT COMPONENTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.