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Sign in to claim this brandCuriteva, LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 25127 WILL MCCOMB DR, Tanner, AL, 35671
- Website
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3012131184
- DUNS Number
- —
Catalogue (1660)
Page 34 of 34| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Curiteva Porous PEEK Laminoplasty System | K243137 | FDA 510(k) | Class II | Active |
| Curiteva Pedicle Screw System | K191810 | FDA 510(k) | Class II | Active |
| Curiteva Sacroiliac Joint Fusion System | K210402 | FDA 510(k) | Class II | Active |
| Curiteva Anterior Cervical Plate System | K181562 | FDA 510(k) | Class II | Active |
| Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System | K252205 | FDA 510(k) | Class II | Active |
| Curiteva Porous PEEK Lumbar Interbody Fusion System | K233744 | FDA 510(k) | Class II | Active |
| Curiteva Thoracolumbar Plate System | K233360 | FDA 510(k) | Class II | Active |
| Curiteva Navigation System | K223200 | FDA 510(k)FDA UDI | Class II | Active |
| Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) | K181549 | FDA 510(k) | Class II | Active |
| Curiteva Cervical Interbody Fusion System | K181261 | FDA 510(k) | Class II | Active |
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