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Bioplate, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
23
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K082757MODIFIED STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH BIOPLATE TITANIUM FIXATION SYSTEMOctober 1, 2008
K082175MOFICATION TO: MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATIONAugust 13, 2008
K070901MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEMJune 15, 2007
K062819BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYDecember 4, 2006
K051845THE BIOPLATE RESORBABLE ENDOBROW FIXATION SYSTEMJuly 27, 2005
K031028THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYApril 28, 2003
K030806BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYApril 8, 2003
K023810MODIFICATION TO BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYDecember 4, 2002
K023665MODIFICATION TO BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYNovember 22, 2002
K022986THE BIOPLATE BATTERY POWERED DRILLNovember 19, 2002
K022890MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLSeptember 6, 2002
K022033STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH THE BIOPLATE TITANIUM FIXATION SYSTEMJuly 19, 2002
K021684THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYJune 26, 2002
K020088MODIFICATION OF THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEMFebruary 8, 2002
K013050THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEMDecember 10, 2001
K013055THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEMDecember 7, 2001
K012908BIOPLATE RESORBABLE BONE SCREWNovember 28, 2001
K012910THE BIOPLATE MANDIBLE FIXATION SYSTEMNovember 20, 2001
K011380MODIFICATION TO THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEMMay 14, 2001
K002426THE BIOPLATE REGID FIXATION BONE PLATING SYSTEM FOR CRANOMAXILLOFACIAL SURGERYJanuary 26, 2001