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Sign in to claim this brandChoicespine, LP
US
Last updated May 23, 2026
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Catalogue (9808)
Page 8 of 197| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| TYPHOON™Facet Screw Fixation System | KT20-4540 | FDA UDI | U | Active |
| HARRIER-SA Lumber Interbody System | S-YT40-Z017 | FDA UDI | Class II | Active |
| Silverbolt/Mainframe | 200-2225 | FDA UDI | Class II | Active |
| Acapella One | 05-099-28-1604 | FDA UDI | Class I | Active |
| LANCER™ Pedicle Screw System | MT60-9570 | FDA UDI | Class II | Active |
| HARRIER™ Choice Spine Intervertebral Body Device | J071-34250620 | FDA UDI | Class I | Active |
| SCS Spinal System | 2T20-CP11 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET10-8570 | FDA UDI | Class II | Active |
| Silverbolt/Mainframe | 200-5545 | FDA UDI | Class II | Active |
| Thunderbolt | MT11-50110-120 | FDA UDI | Class II | Active |
| LANCER™/THUNDERBOLT™ Pedicle Screw System | M070-0022 | FDA UDI | Class I | Active |
| HARRIER™ Choice Spine Intervertebral Body Device | J071-34250021 | FDA UDI | Class I | Active |
| VEO® Lateral Interbody Fusion System | 20-3450 | FDA UDI | Class I | Active |
| HARRIER™ Choice Spine Intervertebral Body Device | JP10-26200415 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET50-8060 | FDA UDI | Class II | Active |
| TOMCAT Cervical Spinal System | S-RH30-1412508 | FDA UDI | Class II | Active |
| STEALTH™ Anterior Cervical Interbody Spacer | DP20-1416611 | FDA UDI | Class II | Active |
| VEO® Lateral Interbody Fusion System | 22-0468-19 | FDA UDI | Class II | Active |
| Silverbolt/Mainframe | 202-2035 | FDA UDI | Class II | Active |
| BLACKBIRD™ Spinal System | LT40-S160 | FDA UDI | Class II | Active |
| Silverbolt/Mainframe | 200-5150 | FDA UDI | Class II | Active |
| THUNDERBOLT™ Minimally Invasive Pedicle Screw Systems | MT10-9575 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET50-8575 | FDA UDI | Class II | Active |
| HARRIER™ Choice Spine Intervertebral Body Device | JP35-34252018 | FDA UDI | Class II | Active |
| Octane A | 602-98-1011 | FDA UDI | Class II | Active |
| Proliant | 05-052-00-0050 | FDA UDI | Class II | Active |
| HARRIER-SA Lumbar Interbody System | S-YT60-30401512 | FDA UDI | Class II | Active |
| BLACKHAWK Cervical Spacer System | S-TT10-1614009 | FDA UDI | Class II | Active |
| Thunderbolt Pedicle Screw System | M070-0132 | FDA UDI | Class I | Active |
| TOMCAT Cervical Spinal System | S-RH20-1614010 | FDA UDI | Class II | Active |
| VEO® Lateral Interbody Fusion System | 22-0469-09 | FDA UDI | Class II | Active |
| BLACKBIRD Spinal System | LT21-3518 | FDA UDI | Class II | Active |
| HARRIER-SA Lumbar Interbody System | S-YT10-26321513 | FDA UDI | Class II | Active |
| HAWKEYE Vertebral Body Replacement (VBR) | WT10-12140055 | FDA UDI | Class II | Active |
| HARPOON™ Lumbar Spacer System | PP40-32124 | FDA UDI | Class II | Active |
| SHARK™ Lumbar Spacer System | PP20-32110 | FDA UDI | Class II | Active |
| Octane Straight PC | 05-072-03-2411 | FDA UDI | Class II | Active |
| VEO® Lateral Interbody Fusion System | V070-0005 | FDA UDI | Class I | Active |
| TOMCAT™ Cervical Spinal System | R070-1412808 | FDA UDI | Class I | Active |
| STARFIRE™ Pedicle Screw System | E070-0032 | FDA UDI | Class I | Active |
| THUNDERBOLT™ Minimally Invasive Pedicle Screw Systems | MC20-P095 | FDA UDI | Class II | Active |
| SHARK™ Lumbar Spacer System | PP10-20154 | FDA UDI | Class II | Active |
| HARRIER-SA Lumbar Interbody System | S-YP10-26321515 | FDA UDI | Class II | Active |
| Acapella One | 05-099-05-1805 | FDA UDI | Class I | Active |
| THUNDERBOLT™ Minimally Invasive and LANCER™ Open Pedicle Screw System | MT80-PEM65 | FDA UDI | Class II | Active |
| VEO® Lateral Interbody Fusion System | 22-0657 | FDA UDI | Class I | Active |
| HAWKEYE™ Vertebral Body Replacement (VBR) | D070-0009 | FDA UDI | Class I | Active |
| Octane T | 600-9109 | FDA UDI | Class I | Active |
| Harrier SA | YT35-5540 | FDA UDI | Class II | Active |
| HARRIER-SA Lumbar Interbody System | S-YP10-28362019 | FDA UDI | Class II | Active |
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