Implant Direct, LLC is one of 21469 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Implant Direct, LLC - FDA 510(k) Cleared Devices
Recent clearances: SPECTRA SYSTEM DENTAL IMPLANTS 2008, SPECTRA-SYSTEM ABUTMENTS 2008, SWISSPLANT DENTAL IMPLANT SYSTEM
10
Total
10
Cleared
0
Denied
Implant Direct, LLC has 10 FDA 510(k) cleared dental devices. Based in Calabasas, US.
Historical record: 10 cleared submissions from 2006 to 2009.
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 - Implant Direct, LLC
10 devices
Cleared
May 15, 2009
SPECTRA SYSTEM DENTAL IMPLANTS 2008
Dental
105d
Cleared
Jan 14, 2009
SPECTRA-SYSTEM ABUTMENTS 2008
Dental
272d
Cleared
Jan 14, 2009
SWISSPLANT DENTAL IMPLANT SYSTEM
Dental
240d
Cleared
Jul 15, 2008
SCREWINDIRECT DENTAL IMPLANTS
Dental
132d
Cleared
May 16, 2008
REACTIVE DENTAL IMPLANT SYSTEM
Dental
64d
Cleared
Mar 07, 2008
REPLUS DENTAL IMPLANTS (HA)
Dental
119d
Cleared
Dec 13, 2007
SCREWPLUS DENTAL IMPLANTS (HA)
Dental
45d
Cleared
Dec 10, 2007
LEGACY DENTAL IMPLANTS
Dental
45d
Cleared
Sep 29, 2006
SPECTRA SYSTEM
Dental
141d
Cleared
May 19, 2006
LEGACY ABUTMENT SYSTEM
Dental
130d