Arthrosurface Incorporated
8 devices · 8 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- HemiCAPOVO® 8156-0032-AProsthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented1 report
- HemiCAPOVO® 8H02-5046-WProsthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented1 report
- Nano fx® FURS-0100Orthopedic Manual Surgical Instrument1 report
- Nano fx® FURS-4101Orthopedic Manual Surgical Instrument1 report
- HemiCAPGRS® G203-2015-AProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 report
- HemiCAPWAVE® PX11-0218-WProsthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer1 report
- UniCAP® US02-4020-WProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer1 report
- UniCAP® US11-0205-WProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer1 report