Ascension Orthopedics, Inc.
45 devices · 74 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.
Ascension Orthopedics, Inc. products
All Ascension Orthopedics, Inc. devices
- Titan™ IMP-0961-064-SORTHOPEDIC MANUAL SURGICAL INSTRUMENT14 reports
- Cadence™ 10204305ORTHOPEDIC MANUAL SURGICAL INSTRUMENT5 reports
- Cadence™ 10208102PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER3 reports
- TITAN™ SZR-0926-030-010TEMPLATE3 reports
- TITAN™ SZR-0926-030-020TEMPLATE3 reports
- Cadence® 10203102ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- Titan™ TRL096002CPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED2 reports
- Titan™ ROD-0923-040-001ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- Titan™ IMP-0926-030-02AIMPACTOR2 reports
- Cadence™ 10203101ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- Ascension® MCP MCP10030PWWFinger Semi-Constrained Pyrolytic Carbon Uncemented Prosthesis1 report
- Ascension PIP PIP-200-20P-WWHigh Demand, Revision, Semi-Constrained, Pyrolytic Carbon, Uncemented Finger Prosthesis1 report
- Universal 2™ Total Wrist System 261301Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained1 report
- Universal 2™ Total Wrist System 263200LFProsthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained1 report
- Integra® Freedom Wrist Arthroplasty System 348292Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained1 report
- Ascension® Silicone PIP SPIP5200WWPROSTHESIS, FINGER, CONSTRAINED, POLYMER1 report
- Ascension® Silicone PIP SPIP5202WWPROSTHESIS, FINGER, CONSTRAINED, POLYMER1 report
- Integra® MemoFix® MS151515STAPLE, FIXATION, BONE1 report
- Titan™ Total Shoulder System B92002012STDPROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED1 report
- Titan™ DTL096008LRGTEMPLATE1 report
- Titan™ HDL096006501ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Titan™ INS096004802TEMPLATE1 report
- Cadence™ 10209208PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Cadence™ 10207101PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Cadence™ 10207112PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Cadence™ 10207203PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 report
- Cadence™ 10206206ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Titan™ DGB096008STDORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Titan™ IMP096006401IMPACTOR1 report
- Titan™ IMP096006601IMPACTOR1 report
- Integra® IMP30000IMPACTOR1 report
- Titan™ IMS096007001ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Integra® MAL092008501ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Integra® RET-920-60RETRACTOR1 report
- Titan™ SCR096006301ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Titan™ SET189D007ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Integra® FGT-305TTEMPLATE1 report
- TITAN™ SZR-0926-030-000TEMPLATE1 report
- TITAN™ SZR-0926-030-030TEMPLATE1 report
- 1 report
- Titan™ IMP-0926-030-00AIMPACTOR1 report
- Titan™ IMP-0926-030-01AIMPACTOR1 report
- Salto Talaris® MJU361TIMPACTOR1 report
- Panta® 2 PAN-1010-10180ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES1 report
- TitanTM INS096009401ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report