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Sign in to claim this brandAvatech Corp.
US
Last updated May 24, 2026
What Avatech Corp. makes
Avatech Corp. manufactures single-use nitrile and vinyl examination gloves, both non-powdered variants, as well as wound care dressings. Their product line includes nonadherent, absorbent wound dressings and adhesive synthetic polymer film dressings designed for skin protection and moisture management. Examples include specific glove and dressing models like TitanFlex and Schneider.
All of Avatech Corp.’s products fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to regulatory requirements for these low-risk devices.
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 Avatech Corp. manufacture?
Avatech Corp. specializes in single-use medical devices primarily for examination, treatment, and wound care. Their product line includes nitrile and vinyl examination gloves (both non-powdered), as well as wound dressings such as nonadherent, absorbent dressings and adhesive synthetic polymer film dressings. These are designed for tasks requiring barrier protection and skin management.
Where is Avatech Corp. based, and how does this affect their devices?
Avatech Corp. is based in the United States. Since their devices fall under FDA Class I classification—considered low-risk—they must comply with U.S. regulatory standards, including listing in the FDA’s Unique Device Identifier (UDI) database. This ensures traceability and transparency for healthcare providers.
Which regulatory registries list Avatech Corp.’s devices?
Avatech Corp.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices, ensuring healthcare professionals and regulators can verify product details like specifications and compliance status.
How are Avatech Corp.’s devices classified by regulatory authorities?
All of Avatech Corp.’s devices are classified as FDA Class I medical devices. This classification is assigned based on risk level—Class I devices are generally considered low-risk and pose minimal harm to users. As a result, they typically require less stringent regulatory oversight compared to higher-risk categories.
Why do Avatech Corp.’s gloves and dressings share the same regulatory classification?
Avatech Corp.’s gloves and dressings are classified as Class I because they are designed for low-risk applications. Examination gloves and nonadherent wound dressings are intended for short-term, controlled use with minimal potential for harm. This classification aligns with their purpose—protection during procedures or minor wound care—without requiring invasive or high-risk features.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- schneidercare.com
- —
- —
- [email protected]
- Phone
- (866) 598-7755
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 073477685
Catalogue (86)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Schneider | VMFC2004 | FDA UDI | Class I | Active |
| Schneider | NBFT7003 | FDA UDI | Class I | Active |
| Schneider | VSFB3013 | FDA UDI | Class I | Active |
| Schneider | NBFT7005 | FDA UDI | Class I | Active |
| Schneider | NBFT7015 | FDA UDI | Class I | Active |
| Schneider | VSFK3100 | FDA UDI | Class I | Active |
| Schneider | VF3044RD | FDA UDI | Class I | Active |
| Schneider | NBFK7104 | FDA UDI | Class I | Active |
| Schneider | CS2045E | FDA UDI | Class I | Active |
| Schneider | NBFK7110 | FDA UDI | Class I | Active |
| Schneider | VSFK3105 | FDA UDI | Class I | Active |
| Schneider | VMFC2014 | FDA UDI | Class I | Active |
| TitanFlex | HD20K00 | FDA UDI | Class I | Active |
| Schneider | VSFB3000 | FDA UDI | Class I | Active |
| Schneider | VMFC2001 | FDA UDI | Class I | Active |
| Schneider | VSFB3014 | FDA UDI | Class I | Active |
| Schneider | VSFB3011 | FDA UDI | Class I | Active |
| Schneider | NBFK7105 | FDA UDI | Class I | Active |
| Schneider | VMFC2003 | FDA UDI | Class I | Active |
| Schneider | VSFB3004 | FDA UDI | Class I | Active |
| Schneider | VSFK3110 | FDA UDI | Class I | Active |
| Schneider | NBFT7002 | FDA UDI | Class I | Active |
| TitanFlex | HD20B13 | FDA UDI | Class I | Active |
| Schneider | NBFK7115 | FDA UDI | Class I | Active |
| Schneider | NBFK7112 | FDA UDI | Class I | Active |
| Schneider | VMFC2010 | FDA UDI | Class I | Active |
| Schneider | NBFT7012 | FDA UDI | Class I | Active |
| Schneider | VSFK3114 | FDA UDI | Class I | Active |
| TitanFlex | HD20K04 | FDA UDI | Class I | Active |
| Schneider | VSFB3010 | FDA UDI | Class I | Active |
| TitanFlex | HD20B15 | FDA UDI | Class I | Active |
| TitanFlex | HD20B14 | FDA UDI | Class I | Active |
| Schneider | NBFT7013 | FDA UDI | Class I | Active |
| TitanFlex | HD20K02 | FDA UDI | Class I | Active |
| Schneider | NBFK7111 | FDA UDI | Class I | Active |
| Schneider | VMFC2002 | FDA UDI | Class I | Active |
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