Friadent GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Friadent GmbH - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Friadent GmbH has 18 FDA 510(k) cleared dental devices. Based in Lake Forest, US.
Historical record: 18 cleared submissions from 1999 to 2004.
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 - Friadent GmbH
18 devices
Cleared
Oct 27, 2004
FRIADENT PLUS DENTAL IMPLANT SYSTEMS
Dental
275d
Cleared
Aug 26, 2004
ANKYLOS DENTAL IMPLANT SYSTEM
Dental
80d
Cleared
Jul 01, 2004
ANKYLOS DENTAL IMPLANT SYSTEM
Dental
80d
Cleared
Oct 02, 2003
XIVE TG ABUTMENTS
Dental
69d
Cleared
Aug 14, 2003
MODIFICATION TO FRIALIT-2 DENTAL IMPLANT SYSTEM
Dental
76d
Cleared
Aug 14, 2003
XIVE DENTAL IMPLANT SYSTEM MULTIPLE
Dental
30d
Cleared
Aug 14, 2003
XIVE TG DENTAL IMPLANT SYSTEM
Dental
21d
Cleared
Mar 03, 2003
XIVE TRANSGINGIVAL DENTAL IMPLANT SYSTEM
Dental
89d
Cleared
Feb 05, 2003
FRIOS ALGIPORE
Dental
83d
Cleared
Jul 02, 2002
XIVE DENTAL IMPLANT SYSTEM
Dental
68d
Cleared
Apr 09, 2002
FRIALOC DENTAL IMPLANT SYSTEM
Dental
209d
Cleared
Mar 15, 2002
XIVE DENTAL IMPLANT SYSTEM
Dental
114d