Bioplate, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Bioplate, Inc. has 23 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 23 cleared submissions from 2000 to 2008. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bioplate, Inc. Filter by specialty or product code using the sidebar.
23 devices
Cleared
Oct 01, 2008
MODIFIED STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH BIOPLATE...
Dental
12d
Cleared
Aug 13, 2008
MOFICATION TO: MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION
Neurology
12d
Cleared
Jun 15, 2007
MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM
Neurology
74d
Cleared
Dec 04, 2006
BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
Neurology
75d
Cleared
Jul 27, 2005
THE BIOPLATE RESORBABLE ENDOBROW FIXATION SYSTEM
Dental
20d
Cleared
Apr 28, 2003
THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
Dental
27d
Cleared
Apr 08, 2003
BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
Dental
26d
Cleared
Dec 04, 2002
MODIFICATION TO BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR...
Dental
19d
Cleared
Nov 22, 2002
MODIFICATION TO BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL...
Dental
22d
Cleared
Nov 19, 2002
THE BIOPLATE BATTERY POWERED DRILL
Neurology
71d
Cleared
Sep 06, 2002
MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING...
Dental
7d
Cleared
Jul 19, 2002
STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH THE BIOPLATE TITANIUM...
Dental
28d