Biodenta Swiss AG
Biodenta Swiss AG holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2015.
Top product codes for Biodenta Swiss AG
Recent clearances by Biodenta Swiss AG
- K151295 — Biodenta Customized Abutment - Titanium
- K150296 — Biodenta Customized Abutment-Hybrid
- K133884 — BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
- K123491 — BIODENTA DENTAL IMPLANT SYSTEM - MULTI-USE ABUTMENT
- K122559 — BIODENTA DENTAL IMPLANT SYSTEM - ABUTMENTS
- K123512 — BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL D 3.0 TO 6.0 MM
- K123415 — BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPERED
- K111003 — BIODENTA DENTAL IMPLANT SYSTEM - BONE LEVEL
- K110778 — BIODENTA CUSTOMIZED ABUTMENT
- K093630 — BIODENTA DENTAL IMPLANT SYSTEM
- K100150 — CERAMICS2IN1
Data sourced from openFDA. This site is unofficial and independent of the FDA.