Is this your brand? Sign in to claim ownership.
Sign in to claim this brandWhat Ulrich GmbH & Co. KG makes
Ulrich GmbH & Co. KG manufactures spinal fixation devices, including non-bioabsorbable bone screws, vertebral body prostheses, and internal spinal fixation systems such as rods, connectors, and plates. Their portfolio also includes spinal interbody fusion cages made of metallic and polymeric materials, as well as orthopaedic fixation system implantation kits for general internal use.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Ulrich GmbH & Co. KG manufacture?
Ulrich GmbH & Co. KG specializes in spinal fixation devices. Their product range includes non-bioabsorbable bone screws, vertebral body prostheses, internal spinal fixation systems (such as rods, connectors, and plates), and spinal interbody fusion cages made from metallic or polymeric materials. They also produce general internal orthopaedic fixation system implantation kits. These devices are designed to support spinal stability and alignment during surgical procedures.
Where is Ulrich GmbH & Co. KG based?
Ulrich GmbH & Co. KG is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution, particularly for FDA-related processes.
Which regulatory registries or databases list Ulrich GmbH & Co. KG’s devices?
Ulrich GmbH & Co. KG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, clinical, and operational purposes, ensuring transparency in the supply chain.
How are Ulrich GmbH & Co. KG’s devices classified under FDA regulations?
Ulrich GmbH & Co. KG’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose the lowest risk and may have fewer regulatory controls, while Class II devices require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and patient exposure.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- ulrichmedical.com
- —
- —
- [email protected]
- Phone
- +4973196540
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 315494757
Catalogue (1391)
Page 3 of 28| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| obeliscPRO™ vertebral body replacement | CS 2914-15 | FDA UDI | Class II | Active |
| tangoRS™ multifunctional posterior system | CS 3008-110 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3807-132 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8008-65-50 | FDA UDI | Class II | Unknown |
| ADD™ anterior distraction device | CS 2250-16-24 | FDA UDI | Class II | Active |
| neon³ CT spinal stabilization | CS 3910-120 | FDA UDI | Class II | Active |
| tangoRS™ multifunctional posterior system | CS 3008-090 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3808-040 | FDA UDI | Class II | Active |
| obeliscPRO™ vertebral body replacement | CS 2914-05 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8008-75-45 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3802-045-030 | FDA UDI | Class II | Active |
| tangoRS™ multifunctional posterior system | CS 3060-7-45 | FDA UDI | Class II | Unknown |
| tezo-T™ titanium cage family | CS 3416-14 | FDA UDI | Class II | Active |
| mambo™ modular cervical plate system | CS 1818-22 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8002-050 | FDA UDI | Class II | Unknown |
| pezo-P™ PEEK cage family | CS 3303-09 | FDA UDI | Class II | Active |
| tangoRS™ multifunctional posterior system | CS 3008-192 | FDA UDI | Class II | Unknown |
| tangoRS™ multifunctional posterior system | CS 3008-375 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3802-045-045 | FDA UDI | Class II | Active |
| tezo-A™ titanium cage family | CS 3434-20 | FDA UDI | Class II | Active |
| golden gate™ anterior plate system | CS 3601-130-A | FDA UDI | Class II | Unknown |
| obelisc | CS 2931-03 | FDA UDI | Class I | Active |
| uCentum™ comprehensive posterior system | CS 3805-085-050 | FDA UDI | Class II | Active |
| ADDplus | CS 1324-1 | FDA UDI | Class II | Active |
| neon™ superior spine system | CS 1402-20T | FDA UDI | Class II | Active |
| obelisc™ vertebral body replacement | CS 2915-00 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8009-65-40 | FDA UDI | Class II | Unknown |
| flamenco™ spinal fixation system | CS 8012-130 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3882-065-055 | FDA UDI | Class II | Active |
| VBR Omni™ vertebral body replacement | CS 2250-30-328 | FDA UDI | Class II | Active |
| obelisc™ vertebral body replacement | CS 2926-05 | FDA UDI | Class II | Active |
| osmium™, ADDplus™ | CS 1303-16 | FDA UDI | Class II | Active |
| Ul_inject | XD 8000 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8012-090 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3802-045-025 | FDA UDI | Class II | Active |
| ulrich medical disposables | XD 10701 | FDA UDI | Class II | Active |
| tezo-T™ titanium cage family | CS 3416-13 | FDA UDI | Class II | Active |
| tezo-A™ titanium cage family | CS 3431-20 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8012-480 | FDA UDI | Class II | Unknown |
| pezo-P™ PEEK cage family | CS 3301-11 | FDA UDI | Class II | Active |
| ADD™ anterior distraction device | CS 2250-16-166 | FDA UDI | Class II | Active |
| tezo-A™ titanium cage family | CS 3431-12 | FDA UDI | Class II | Active |
| neon³™ OCT spinal stabilization | CS 3917-12 | FDA UDI | Class II | Active |
| flamenco™ spinal fixation system | CS 8007-65-40 | FDA UDI | Class II | Unknown |
| VBR Omni™ vertebral body replacement | CS 2250-19-724 | FDA UDI | Class II | Active |
| uCentum™ comprehensive posterior system | CS 3882-045-050 | FDA UDI | Class II | Active |
| VBR Omni™ vertebral body replacement | CS 2250-22-324 | FDA UDI | Class II | Active |
| uCentum™ comprehensive posterior system | CS 3882-085-055 | FDA UDI | Class II | Active |
| VBR™ vertebral body replacement | CS 2228-821302 | FDA UDI | Class II | Unknown |
| uCentum™ comprehensive posterior system | CS 3884-065-050 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.