Is this your brand? Sign in to claim ownership.
Sign in to claim this brandSpinal Kinetics, LLC
US
Last updated May 23, 2026
What Spinal Kinetics, LLC makes
Spinal Kinetics, LLC produces modular cervical total intervertebral disc prostheses, designed for spinal replacement surgery, as well as reusable and single-use orthopaedic surgical procedure kits for spinal procedures. Their modular disc prostheses are intended for cervical spine applications, while the surgical kits support procedural preparation and execution in orthopaedic settings.
The company’s products are regulated under FDA classifications, including Class I, Class II, and Class III devices, with authorisations obtained through 510(k), PMA, and UDI registrations. These devices are listed in the FDA’s regulatory databases, and the company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (87)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| M6-C | FA 0192-06 | FDA UDI | Class I | Active |
| M6-C | FA 0201 | FDA UDI | Class I | Active |
| M6-C | 7ML | FDA UDI | Class III | Active |
| M6-C | FA 0290 | FDA UDI | Class II | Active |
| M6-C | FA 0193-07 | FDA UDI | Class II | Active |
| M6-C | FA 0207-02 | FDA UDI | Class II | Active |
| M6-C | FA 0193-06 | FDA UDI | Class II | Active |
| M6-C | FA 0193-05 | FDA UDI | Class III | Active |
| M6-C | FA 0192-02 | FDA UDI | Class I | Active |
| M6-C | 1503-2070.90 | FDA UDI | Class II | Active |
| M6-C | FA 0208-04 | FDA UDI | Class I | Active |
| M6-C | FA 0208-05 | FDA UDI | Class I | Active |
| M6-C | FA 0205 | FDA UDI | Class II | Active |
| M6-C | FA 0193-04 | FDA UDI | Class II | Active |
| M6-C | FA 0194-02 | FDA UDI | Class II | Active |
| M6-C | 7M | FDA UDI | Class III | Active |
| M6-C | FA 0196 | FDA UDI | Class II | Active |
| M6-C | FA 0198 | FDA UDI | Class I | Active |
| M6-C | FA 0050-02 | FDA UDI | Class I | Active |
| M6-C | FA 0208-07 | FDA UDI | Class I | Active |
| M6-C | FA 0192-07 | FDA UDI | Class I | Active |
| M6-C | 6LL | FDA UDI | Class III | Active |
| M6-C | 7LL | FDA UDI | Class III | Active |
| M6-C | FA 0192-04 | FDA UDI | Class I | Active |
| M6-C | FA 0051 | FDA UDI | Class I | Active |
| M6-C | 1503-2010.90 | FDA UDI | Class II | Active |
| M6-C | FA 0209-02 | FDA UDI | Class II | Active |
| M6-C | PK 0247 | FDA UDI | Class II | Active |
| M6-C | 1503-2020.90 | FDA UDI | Class II | Active |
| M6-C | 1503-2080.90 | FDA UDI | Class II | Active |
| M6-C | FA 0189 | FDA UDI | Class I | Active |
| M6-C | FA 0200 | FDA UDI | Class I | Active |
| M6-C | FA 0208-03 | FDA UDI | Class I | Active |
| M6-C | FA 0207-01 | FDA UDI | Class II | Active |
| M6-C | FG 0167 | FDA UDI | Class II | Active |
| M6-C Artificial Cervical Disc Instruments AS | K220861 | FDA 510(k) | Class II | Active |
| M6-C Artificial Cervical Disc | P170036 | FDA PMA | Class III | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.