Biodenta Swiss AG

11FDA 510(k) medical device clearances.

Top product codes for Biodenta Swiss AG

DZE — Dental5 devices
NHA — Dental5 devices
EIH — Dental1 device

Recent clearances by Biodenta Swiss AG

K151295 — Biodenta Customized Abutment - TitaniumCode NHA·2015-12-01
K150296 — Biodenta Customized Abutment-HybridCode NHA·2015-07-02
K133884 — BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MMCode DZE·2014-06-13
K123491 — BIODENTA DENTAL IMPLANT SYSTEM - MULTI-USE ABUTMENTCode NHA·2013-05-30
K122559 — BIODENTA DENTAL IMPLANT SYSTEM - ABUTMENTSCode NHA·2013-05-03
K123512 — BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL D 3.0 TO 6.0 MMCode DZE·2013-03-28
K123415 — BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPEREDCode DZE·2013-03-19
K111003 — BIODENTA DENTAL IMPLANT SYSTEM - BONE LEVELCode DZE·2011-09-15
K110778 — BIODENTA CUSTOMIZED ABUTMENTCode NHA·2011-07-29
K093630 — BIODENTA DENTAL IMPLANT SYSTEMCode DZE·2010-06-03
K100150 — CERAMICS2IN1Code EIH·2010-05-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.