Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by BIODENTA SWISS AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110778
03/21/2011
BIODENTA CUSTOMIZED ABUTMENT
BIODENTA SWISS AG
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
K150296
02/06/2015
Biodenta Customized Abutment-Hybrid
BIODENTA SWISS AG
K151295
05/15/2015
Biodenta Customized Abutment - Titanium
BIODENTA SWISS AG
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact