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Avatech 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
—
LinkedIn
—
Facebook
—
Phone
(866) 598-7755
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
073477685

Catalogue (86)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
TitanFlex HD20B10
FDA UDI
Class IActive
Schneider VMFC2011
FDA UDI
Class IActive
Schneider NBFT7010
FDA UDI
Class IActive
Schneider VSFB3003
FDA UDI
Class IActive
Schneider VMFC2005
FDA UDI
Class IActive
Schneider VSFK3113
FDA UDI
Class IActive
TitanFlex HD20B11
FDA UDI
Class IActive
TitanFlex HD20B03
FDA UDI
Class IActive
Schneider VSFB3001
FDA UDI
Class IActive
Schneider NBFT7014
FDA UDI
Class IActive
Schneider VSFB3002
FDA UDI
Class IActive
TitanFlex HD20B04
FDA UDI
Class IActive
Schneider VSFB3005
FDA UDI
Class IActive
Schneider VF3077SP
FDA UDI
Class IActive
Schneider VF3022RD
FDA UDI
Class IActive
TitanFlex HD20K11
FDA UDI
Class IActive
TitanFlex HD20K05
FDA UDI
Class IActive
Schneider NBFT7011
FDA UDI
Class IActive
Schneider VMFC2015
FDA UDI
Class IActive
Schneider CS2068I
FDA UDI
Class IActive
TitanFlex HD20K13
FDA UDI
Class IActive
Schneider VSFK3111
FDA UDI
Class IActive
Schneider VMFC2013
FDA UDI
Class IActive
Schneider VF3033RD
FDA UDI
Class IActive
Schneider NBFK7102
FDA UDI
Class IActive
TitanFlex HD20K10
FDA UDI
Class IActive
TitanFlex HD20K15
FDA UDI
Class IActive
TitanFlex HD20B00
FDA UDI
Class IActive
Schneider VSFK3103
FDA UDI
Class IActive
Schneider NBFK7114
FDA UDI
Class IActive
Schneider NBFT7001
FDA UDI
Class IActive
TitanFlex HD20B01
FDA UDI
Class IActive
Schneider NBFK7113
FDA UDI
Class IActive
Schneider NBFK7103
FDA UDI
Class IActive
TitanFlex HD20K03
FDA UDI
Class IActive
Schneider VSFK3102
FDA UDI
Class IActive
TitanFlex HD20B05
FDA UDI
Class IActive
Schneider NBFT7000
FDA UDI
Class IActive
Schneider NBFK7100
FDA UDI
Class IActive
TitanFlex HD20B12
FDA UDI
Class IActive
TitanFlex HD20K01
FDA UDI
Class IActive
Schneider VSFK3115
FDA UDI
Class IActive
Schneider VSFK3104
FDA UDI
Class IActive
Schneider VMFC2000
FDA UDI
Class IActive
Schneider NBFT7004
FDA UDI
Class IActive
TitanFlex HD20K14
FDA UDI
Class IActive
Schneider VSFK3101
FDA UDI
Class IActive
Schneider VF3044RP
FDA UDI
Class IActive
Schneider VSFB3015
FDA UDI
Class IActive
Schneider NBFK7101
FDA UDI
Class IActive

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