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Sign in to claim this brandInnovision, Inc
US
Last updated May 24, 2026
What Innovision, Inc makes
Innovision, Inc manufactures orthopaedic fixation devices, including non-bioabsorbable bone screws and sterile bone washers, as well as bone access cannulas. Their portfolio includes the N-Force 7.3 and N-Force 4.0 fixation systems, designed for internal fixation in orthopaedic procedures.
The company’s devices are regulated under FDA classifications, with products falling into Class I and Class II categories. They are listed in the FDA’s 510(k) and UDI registries, and 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 Innovision, Inc manufacture?
Innovision, Inc specializes in orthopaedic fixation devices. Their portfolio includes non-bioabsorbable bone screws (sterile), orthopaedic bone washers (sterile), and bone access cannulas. These products are primarily used for internal fixation in orthopaedic surgical procedures, such as fracture stabilization or joint repair.
Where is Innovision, Inc based?
Innovision, Inc is headquartered in the United States. The company’s location is relevant for regulatory oversight, as its devices are subject to FDA requirements and classifications.
Which regulatory registries list Innovision, Inc’s devices?
Innovision, Inc’s devices are included in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) registry. These registries track devices that have undergone FDA review for compliance with applicable regulations, ensuring transparency in their regulatory status.
How are Innovision, Inc’s devices classified under FDA regulations?
Innovision, Inc’s devices fall into Class I and Class II categories under FDA classification. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and require special controls to ensure safety and effectiveness. The specific classification depends on the device’s intended use and potential risks.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- zimmberbiomet.com
- —
- —
- [email protected]
- Phone
- 1(800)348-2759
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 942243767
Catalogue (63)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| N-Force 7.3 Fixation System | IN027-80-FS | FDA UDI | Class II | Active |
| N-Force 4.0 Fixation System | IN001-65-FS | FDA UDI | Class II | Active |
| N-Force 4.0 Fixation System | IN006-75-FS | FDA UDI | Class II | Active |
| N-Force 7.3 Fixation System | IN038-95-FS | FDA UDI | Class II | Active |
| N-Force 7.3 Fixation System | IN038-75-FS | FDA UDI | Class II | Active |
| N-Force 4.0 Fixation System | IN001-50-FS | FDA UDI | Class II | Active |
| N-Force 7.3 Fixation System | IN038-105-FS | FDA UDI | Class II | Active |
| Accucon | K944223 | FDA 510(k) | Class II | Active |
| Hydro2, Hs-75 | K011914 | FDA 510(k) | Class II | Active |
| N-Force Fixation System | K102528 | FDA 510(k) | Class II | Active |
| Hydro2, Hs-75 | K000485 | FDA 510(k) | Class II | Active |
| N-Force Fixation System | K132244 | FDA 510(k) | Class II | Active |
| N-Force Fixation System | K151146 | FDA 510(k) | Class II | Active |
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