Handpiece, Rotary Bone Cutting
FDA product code KMW · Class 2 · 16 devices · 46 reports · 0 devices named in recalls
- OsteoMed 450-0241Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING9 reports
- Surgical Straight Handpiece SGS-E2SNakanishi Inc. · Handpiece, Rotary Bone Cutting8 reports
- OsteoMed 450-0034Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING6 reports
- OsteoMed 450-0021-00Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING3 reports
- OsteoMed 450-0084Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING3 reports
- OsteoMed 450-0390Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING3 reports
- S-12 surgical handpiece 1:2 30061000W & H Dentalwerk Bürmoos GmbH · Handpiece, Rotary Bone Cutting3 reports
- SGA-E2SNakanishi Inc. · HANDPIECE, ROTARY BONE CUTTING2 reports
- S-11 surgical handpiece 1:1 30056000W & H Dentalwerk Bürmoos GmbH · Handpiece, Rotary Bone Cutting2 reports
- OsteoMed 220-0302Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING1 report
- OsteoMed 450-0005-00Osteomed LLC · HANDPIECE, ROTARY BONE CUTTING1 report
- Ti-Max X X-SG93LNakanishi Inc. · HANDPIECE, ROTARY BONE CUTTING1 report
- Ti-Max X X-SG93Nakanishi Inc. · HANDPIECE, ROTARY BONE CUTTING1 report
- Ti-Max X X-SG65LNakanishi Inc. · HANDPIECE, ROTARY BONE CUTTING1 report
- Ti-Max X X-DSG20LNakanishi Inc. · HANDPIECE, ROTARY BONE CUTTING1 report
- Screw driver angled 90° 30014000W & H Dentalwerk Bürmoos GmbH · Handpiece, Rotary Bone Cutting1 report