Probe
FDA product code HXB · Class 1 · 61 devices · 279 reports · 1 deaths reported · 2 devices named in recalls
- EXPEDIUM 279702030Depuy Spine, LLC · PROBE53 reports
- Sklar Instruments 94-5923Sklar Corporation · PROBE1 recall0 reports
- Sklar 96-2361Sklar Corporation · PROBE1 recall0 reports
- MOSS 275010140Depuy Spine, LLC · PROBE28 reports
- EXPEDIUM 279702040Depuy Spine, LLC · PROBE21 reports
- MULTILOC 03.019.029Synthes GmbH · PROBE15 reports
- MOSS 275010160Depuy Spine, LLC · PROBE11 reports
- EXPEDIUM 279702010Depuy Spine, LLC · PROBE9 reports
- EXPEDIUM 279702070Medos International Sàrl · PROBE9 reports
- EXPEDIUM 299704125Medos International Sàrl · PROBE8 reports
- Xenon 22SPT09Alphatec Spine, Inc. · PROBE7 reports
- Xenon 22SPT10Alphatec Spine, Inc. · PROBE7 reports
- VSP 202549Depuy Spine, LLC · PROBE7 reports
- Vitality® 07.02072.001Zimmer Spine, Inc. · PROBE6 reports
- NA 9400-80-001Depuy (Ireland) · PROBE6 reports
- EXPEDIUM 299704130Medos International Sàrl · PROBE6 reports
- N/A 8350294Medtronic Sofamor Danek, Inc. · PROBE5 reports
- Vitality® 07.02117.001Zimmer Spine, Inc. · PROBE5 reports
- VIPER 286710116Depuy Spine, LLC · PROBE5 reports
- Invictus 17001-01Alphatec Spine, Inc. · PROBE4 reports
- JOURNEY 74018903Smith & Nephew, Inc. · PROBE4 reports
- EXPEDIUM 299704115Medos International Sàrl · PROBE4 reports
- EXPEDIUM 299704110Medos International Sàrl · PROBE4 reports
- NA 00-7050-034-00Zimmer Trabecular Metal Technology Inc. · PROBE3 reports
- uCentum UL 8527-23Ulrich GmbH & Co. KG · Probe3 reports
- MONARCH 277010140Depuy Spine, LLC · PROBE3 reports
- NA 698340577Depuy Spine, LLC · PROBE3 reports
- EXPEDIUM 299704105Medos International Sàrl · PROBE3 reports
- N/A 8350292Medtronic Sofamor Danek, Inc. · PROBE2 reports
- CD HORIZON® Spinal System 25000200Medtronic Sofamor Danek, Inc. · PROBE2 reports
- Vitality® 07.02067.001Zimmer Spine, Inc. · PROBE2 reports
- NA 4862-00-050Depuy (Ireland) · PROBE2 reports
- NA 698202545Depuy Spine, LLC · PROBE2 reports
- NA 288242Medos International Sàrl · PROBE2 reports
- Malibu 91-6117Seaspine Orthopedics Corporation · PROBE2 reports
- Invictus 17003Alphatec Spine, Inc. · PROBE1 report
- N/A 8350293Medtronic Sofamor Danek, Inc. · PROBE1 report
- CD HORIZON® Spinal System 25000300Medtronic Sofamor Danek, Inc. · PROBE1 report
- N/A 803-290Medtronic Sofamor Danek, Inc. · PROBE1 report
- Medtronic Reusable Instruments X0601003Medtronic Sofamor Danek, Inc. · PROBE1 report
- N/A 7480110Medtronic Sofamor Danek, Inc. · PROBE1 death1 report
- Response 5.5/6.0 Cannulated Screw System 01-1301-6021Orthopediatrics Corp. · PROBE1 report
- Illico 73746Alphatec Spine, Inc. · PROBE1 report
- Polaris 4.75 Spinal System 14-510054Zimmer Biomet Inc · Probe1 report
- VITALITY® 730M1001Biomet Spine LLC · PROBE1 report
- VITALITY® 730M1004Biomet Spine LLC · PROBE1 report
- Virage™ 07.01759.001Zimmer Biomet Inc · PROBE1 report
- Arthrex® AR-10100NArthrex, Inc. · PROBE1 report
- Vitality® 07.02077.001Zimmer Spine, Inc. · PROBE1 report
- AESCULAP FW249RAesculap AG · PROBE1 report
- Probe, Articulating 259-695-001RZ-Medizintechnik GmbH · Probe1 report
- NA L94018Depuy (Ireland) · PROBE1 report
- VIPER 286710200Depuy Spine, LLC · PROBE1 report
- NA 698328595Depuy Spine, LLC · PROBE1 report
- NA 698334917Depuy Spine, LLC · PROBE1 report
- NA 698336915Depuy Spine, LLC · PROBE1 report
- NA 03.614.012Synthes GmbH · PROBE1 report
- NA 03.614.013Synthes GmbH · PROBE1 report
- NA 388.54Synthes GmbH · PROBE1 report
- NA 388.544Synthes GmbH · PROBE1 report
- NA 388.545Synthes GmbH · PROBE1 report