FDA 510(k) Applications Submitted by DAVID EILER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100150	01/19/2010	CERAMICS2IN1	BIODENTA SWISS AG
K111003	04/11/2011	BIODENTA DENTAL IMPLANT SYSTEM - BONE LEVEL	BIODENTA SWISS AG
K122559	08/22/2012	BIODENTA DENTAL IMPLANT SYSTEM - ABUTMENTS	BIODENTA SWISS AG
K123415	11/05/2012	BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPERED	BIODENTA SWISS AG
K123491	11/13/2012	BIODENTA DENTAL IMPLANT SYSTEM - MULTI-USE ABUTMENT	BIODENTA SWISS AG
K123512	11/13/2012	BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL D 3.0 TO 6.0 MM	BIODENTA SWISS AG
K093630	11/23/2009	BIODENTA DENTAL IMPLANT SYSTEM	BIODENTA SWISS AG
K133884	12/20/2013	BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM	BIODENTA SWISS AG