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Sign in to claim this brandVisionAir Solutions
US
Last updated September 17, 2026
What VisionAir Solutions makes
VisionAir Solutions manufactures polymeric tracheal and bronchial stents that are non-bioabsorbable, including the VisionAir 3D Stent.
These devices are classified as Class II medical devices and are listed in the FDA UDI registry; the company 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 does VisionAir Solutions make?
VisionAir Solutions manufactures polymeric tracheal and bronchial stents that are non-bioabsorbable, including the VisionAir 3D Stent, as stated in the device data summary.
Where is VisionAir Solutions based?
VisionAir Solutions is based in the United States, as indicated by the COUNTRY field in the device data.
Which registries list VisionAir Solutions' devices?
VisionAir Solutions' devices are listed in the FDA UDI registry, as specified in the LISTED IN field of the device data.
How are VisionAir Solutions' devices classified?
VisionAir Solutions' devices are classified as Class II medical devices, as stated in the DEVICE CLASSES field of the device data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 1800 Triplett Blvd, Akron, OH, 44306
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3010197296
- DUNS Number
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Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VisionAir 3D Stent | 1 | FDA UDI | Class II | Active |
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