Biodenta Swiss AG is one of 79 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Biodenta Swiss AG - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Biodenta Swiss AG has 11 FDA 510(k) cleared dental devices. Based in Berneck, St.Gallen, CH.
Historical record: 11 cleared submissions from 2010 to 2015.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biodenta Swiss AG
11 devices
Cleared
Dec 01, 2015
Biodenta Customized Abutment - Titanium
Dental
200d
Cleared
Jul 02, 2015
Biodenta Customized Abutment-Hybrid
Dental
146d
Cleared
Jun 13, 2014
BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
Dental
175d
Cleared
May 30, 2013
BIODENTA DENTAL IMPLANT SYSTEM - MULTI-USE ABUTMENT
Dental
198d
Cleared
May 03, 2013
BIODENTA DENTAL IMPLANT SYSTEM - ABUTMENTS
Dental
254d
Cleared
Mar 28, 2013
BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL D 3.0 TO 6.0 MM
Dental
135d
Cleared
Mar 19, 2013
BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPERED
Dental
134d
Cleared
Sep 15, 2011
BIODENTA DENTAL IMPLANT SYSTEM - BONE LEVEL
Dental
157d
Cleared
Jul 29, 2011
BIODENTA CUSTOMIZED ABUTMENT
Dental
130d
Cleared
Jun 03, 2010
BIODENTA DENTAL IMPLANT SYSTEM
Dental
192d
Cleared
May 25, 2010
CERAMICS2IN1
Dental
126d