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Sign in to claim this brandWhat Alleva Medical, Ltd. makes
Alleva Medical, Ltd. manufactures negative-pressure wound therapy systems, including foam dressings, canisters, drapes, and reusable electric systems, as well as thoracic suction collection containers.
The company's products are Class II devices listed in the FDA 510(k) and FDA UDI registries, and the company is based in the US.
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 Alleva Medical, Ltd. manufacture?
Alleva Medical, Ltd. produces a range of negative‑pressure wound therapy (NPWT) products, including foam dressings that are non‑antimicrobial, canisters for fluid collection, reusable electric NPWT systems, and drapes that seal the wound area. In addition, the company makes thoracic suction collection containers for chest drainage. This answer is based directly on the device categories listed in the provided data.
Where is Alleva Medical, Ltd. headquartered?
The data specifies that Alleva Medical, Ltd. is based in the United States. No other location information is given, so the answer reflects only the country listed in the source.
Which regulatory registries list Alleva Medical’s devices?
Alleva Medical’s devices appear in the FDA 510(k) and FDA UDI registries. The source explicitly states that the company’s products are listed in these two FDA databases, indicating where the device submissions and unique identifiers are recorded.
How are Alleva Medical’s devices classified under FDA regulations?
All of the devices described—foam dressings, canisters, drapes, reusable electric systems, and thoracic suction containers—are classified as Class II devices. This classification is directly taken from the ‘DEVICE CLASSES’ entry in the supplied information.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
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Catalogue (21)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vide | ST382-0001 | EUDAMEDFDA UDI | Class II | Active |
| ExtriCARE | MI424-0001 | FDA UDI | Class II | Active |
| Vide | ST422-0001 | EUDAMEDFDA UDI | Class II | Active |
| ExtriCARE | MI390-0001 | FDA UDI | Class II | Active |
| ExtriCARE | MI425-0001 | FDA UDI | Class II | Active |
| ExtriCARE | ST391-0001 | FDA UDI | Class II | Active |
| ExtriCARE | MI423-0001 | FDA UDI | Class II | Active |
| ExtriCARE | ST403-0001 | FDA UDI | Class II | Active |
| Vide | ST380-0001 | FDA UDI | Class II | Active |
| ExtriCARE | ST407-0001 | FDA UDI | Class II | Active |
| ExtriCARE | MI391-0002 | FDA UDI | Class II | Active |
| ExtriCARE | MI393-0001 | FDA UDI | Class II | Active |
| ExtriCARE | ST390-0001 | FDA UDI | Class II | Active |
| ExtriCARE | ST397-0001 | FDA UDI | Class II | Active |
| ExtriCARE | ST396-0001 | FDA UDI | Class II | Active |
| Vide | ST423-0001 | EUDAMEDFDA UDI | Class II | Active |
| ExtriCARE | ST394-0001 | FDA UDI | Class II | Active |
| Vide | ST380-0006 | FDA UDI | Class II | Active |
| ExtriCARE | MI392-0001 | FDA UDI | Class II | Active |
| Plexus | K191107 | FDA 510(k) | Class II | Active |
| extriCARE 1000 Negative Pressure Wound Therapy System | K213906 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Alleva Medical (d.g.) Ltd Dongguan City Guangdong · CN FEI 3010308146