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Sign in to claim this brandChoicespine, LP
US
Last updated May 23, 2026
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Catalogue (9808)
Page 4 of 197| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tiger Shark System | P070-24116 | FDA UDI | Class II | Active |
| HARRIER™ Choice Spine Intervertebral Body Device | J072-38272018 | FDA UDI | Class I | Active |
| Harrier-SA Lumbar Interbody System | Y070-30401515C | FDA UDI | Class I | Active |
| Triton | Q070-0016 | FDA UDI | Class I | Active |
| TOMCAT Cervical Spinal System | S-RH20-1614807 | FDA UDI | Class II | Active |
| THUNDERBOLT Minimally Invasive Pedicle Screw Systems | MT10-115110 | FDA UDI | Class II | Active |
| Thunderbolt | M070-0204 | FDA UDI | Class I | Active |
| Triton Si Fixation | Q070-0006 | FDA UDI | Class I | Active |
| TOMCAT Cervical Spinal System | S-RH30-1412412 | FDA UDI | Class II | Active |
| Proliant | 05-054-00-5060 | FDA UDI | Class II | Active |
| TOMCAT™ Cervical Spinal System | R070-N1412508 | FDA UDI | Class I | Active |
| Altes | 27304-025 | FDA UDI | Class II | Active |
| HARRIER-SA Lumbar Interbody System | S-YT10-30401015 | FDA UDI | Class II | Active |
| Silverbolt/Mainframe | 200-2280 | FDA UDI | Class II | Active |
| SHARK Lumbar Spacer System | PT22-22154 | FDA UDI | Class II | Active |
| HAWKEYE Vertebral Body Replacement (VBR) | WT10-12140021 | FDA UDI | Class II | Active |
| Choice Spine Lumbar Spacer System (SABRE™, SHARK™, HORNET™, HARPOON™) | P070-6015 | FDA UDI | Class I | Active |
| LANCER™/THUNDERBOLT™ Pedicle Screw System | MC20-P185 | FDA UDI | Class II | Active |
| ORIA XENA® Top Clip System | CT10-BP845 | FDA UDI | Class II | Active |
| HARRIER™ Choice Spine Intervertebral Body Device | JP50-42300621 | FDA UDI | Class II | Active |
| Acapella One | 05-099-01-0006 | FDA UDI | Class I | Active |
| LANCER™ Pedicle Screw System | MT60-6575 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET50-8590 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET50-5545 | FDA UDI | Class II | Active |
| VEO® Lateral Interbody Fusion System | V070-0041 | FDA UDI | Class I | Active |
| STARFIRE™ Pedicle Screw System | ET50-8540 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET10-8575 | FDA UDI | Class II | Active |
| Octane A | 602-98-1211 | FDA UDI | Class II | Active |
| Octane M | 05-041-02-3013 | FDA UDI | Class II | Active |
| HydraLok | PS70050 | FDA UDI | Class II | Active |
| STARFIRE™ Pedicle Screw System | ET10-6070 | FDA UDI | Class II | Active |
| HAWKEYE Vertebral Body Replacement (VBR) | WT10-14160017 | FDA UDI | Class II | Active |
| HAWKEYE Vertebral Body Replacement (VBR) | WT10-12140030 | FDA UDI | Class II | Active |
| BLACKBIRD™ Spinal System | LT40-P060 | FDA UDI | Class II | Active |
| Choice Spine Lumbar Spacer System (SABRE™, SHARK™, HORNET™, HARPOON™) | T070-32110S | FDA UDI | Class I | Active |
| Silverbolt/Mainframe | 200-0630 | FDA UDI | Class II | Active |
| TOMCAT™ Cervical Spinal System | RH30-1412412 | FDA UDI | Class II | Active |
| LANCER™/THUNDERBOLT™ Pedicle Screw System | M070-0059 | FDA UDI | Class I | Active |
| Choice Spine Lumbar Spacer System (SABRE™, SHARK™, HORNET™, HARPOON™) | P070-2110 | FDA UDI | Class I | Active |
| HARPOON™ Lumbar Spacer System | PP42-28084 | FDA UDI | Class II | Active |
| THUNDERBOLT Minimally Invasive Pedicle Screw Systems | MT32-10565 | FDA UDI | Class II | Active |
| Gibralt | 05-009-12-2720 | FDA UDI | Class I | Active |
| FALCON™ Anterior Cervical Plate | AT10-3052 | FDA UDI | Class II | Active |
| VEO® Lateral Interbody Fusion System | 21-0772 | FDA UDI | Class I | Active |
| LANCER Pedicle Screw System | MT30-11540 | FDA UDI | Class II | Active |
| VEO Lateral Interbody Fusion System | VT10-40170007 | FDA UDI | Class II | Active |
| Choice Spine Lumbar Spacer System (SABRE™, SHARK™, HORNET™, HARPOON™) | T070-28084 | FDA UDI | Class I | Active |
| Ambassador Cervical Plate System | 05-109-02-2002 | FDA UDI | Class I | Active |
| TOMCAT Cervical Spinal System | S-RH30-1616007 | FDA UDI | Class II | Active |
| Gibralt | 05-000-20-4030 | FDA UDI | Class II | Active |
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