Intra-Lock International is one of 5184 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intra-Lock International - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Intra-Lock International has 8 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Historical record: 8 cleared submissions from 2002 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Intra-Lock International Filter by specialty or product code using the sidebar.
Intra-Lock International — FDA 510(k) Products and Clearance History
8 devices
Cleared
Aug 01, 2013
INTRA-LOCK OP DENTAL IMPLANT
Dental
191d
Cleared
May 21, 2008
MINI DRIVE-LOCK DENTAL IMPLANT SYSTEM PROSTHETICS
Dental
79d
Cleared
Oct 12, 2007
MINI DRIVE-LOCK DENTAL IMPLANT SYSTEM
Dental
224d
Cleared
Oct 14, 2005
MILO DENTAL IMPLANT SYSTEM
Dental
179d
Cleared
Mar 22, 2004
INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS
Dental
52d
Cleared
Dec 23, 2003
INTRA-LOCK HYDROXYAPATITE COATED IMPLANTS
Dental
242d
Cleared
Dec 19, 2002
TRANSITIONAL IMPLANTS
Dental
191d
Cleared
Jul 24, 2002
ENDOSSOUS IMPLANTS
Dental
90d