Bioplate, Inc.
FDA 510(k) medical device clearances.
Top product codes for Bioplate, Inc.
Recent clearances by Bioplate, Inc.
- K082757 — MODIFIED STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH BIOPLATE TITANIUM FIXATION SYSTEM
- K082175 — MOFICATION TO: MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION
- K070901 — MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM
- K062819 — BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K051845 — THE BIOPLATE RESORBABLE ENDOBROW FIXATION SYSTEM
- K031028 — THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K030806 — BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K023810 — MODIFICATION TO BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K023665 — MODIFICATION TO BIOPLATE RIGID BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K022986 — THE BIOPLATE BATTERY POWERED DRILL
- K022890 — MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K022033 — STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH THE BIOPLATE TITANIUM FIXATION SYSTEM
- K021684 — THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
- K020088 — MODIFICATION OF THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM
- K013050 — THE BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM
- K013055 — THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
- K012908 — BIOPLATE RESORBABLE BONE SCREW
- K012910 — THE BIOPLATE MANDIBLE FIXATION SYSTEM
- K011380 — MODIFICATION TO THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
- K002426 — THE BIOPLATE REGID FIXATION BONE PLATING SYSTEM FOR CRANOMAXILLOFACIAL SURGERY
- K994060 — THE BIOPLATE RESORBABLE BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY, BIOLACTATE
- K002879 — MODIFICATION TO BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
- K001530 — THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.