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Sign in to claim this brandWhat Inventorr MD Inc makes
Inventorr MD Inc produces medical devices such as skin-closure adhesive strips, including the AbClo device. These products are used for wound closure. The company's devices are types of medical adhesives.
The company's portfolio is regulated as Class I devices and is listed in the FDA UDI registry. The devices are subject to regulatory oversight in the US, where the company is based.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What type of medical devices does Inventorr MD Inc produce?
Inventorr MD Inc produces skin-closure adhesive strips, such as the AbClo device, which are used for wound closure. These devices fall under the category of medical adhesives and are designed to hold wound edges together without sutures or staples. The company's product line is focused on this specific type of device, as indicated in the provided data.
Where is Inventorr MD Inc based?
Inventorr MD Inc is based in the United States, as specified in the COUNTRY field of the device data. The company operates within the U.S. regulatory framework, and its devices are subject to oversight by U.S. authorities, particularly the FDA, given the listing in the FDA UDI registry.
In which regulatory registry are Inventorr MD Inc's devices listed?
Inventorr MD Inc's devices are listed in the FDA UDI registry, as stated in the LISTED IN field. This registry is maintained by the U.S. Food and Drug Administration and contains unique device identification information for medical devices marketed in the United States. The listing indicates that the company's devices comply with U.S. device identification requirements.
How are Inventorr MD Inc's devices classified under regulatory systems?
Inventorr MD Inc's devices are classified as Class I medical devices, as indicated in the DEVICE CLASSES field. Class I devices are subject to the lowest level of regulatory control, typically requiring general controls such as adherence to good manufacturing practices and labeling requirements, but not premarket approval. This classification applies to products like skin-closure adhesive strips based on their risk profile.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- 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
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- DUNS Number
- 204358506
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| AbClo | ABCLO001 | FDA UDI | Class I | Active |
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