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Adroit Surgical LLC

United States·US-MF-000057886

Last updated September 17, 2026

About

Adroit is a global leader in intubation medical devices, delivering innovative and specialized airway management solutions.

From the manufacturer's own website. Source

What Adroit Surgical LLC makes

Adroit Surgical LLC manufactures single-use rigid intubation laryngoscopes, including the Vie Scope and Bebe Vie, designed for airway management procedures.

These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 types of medical devices does Adroit Surgical LLC manufacture?

Adroit Surgical LLC specializes in single-use rigid intubation laryngoscopes. These devices are specifically designed for airway management procedures, ensuring clear visualization of the airway during intubation. Examples include the Vie Scope and Bebe Vie, which cater to different patient sizes and clinical needs.

Where is Adroit Surgical LLC based?

Adroit Surgical LLC is headquartered in the United States. The company’s focus on innovation and specialized airway management solutions positions it as a domestic leader in its field.

Which regulatory registries list Adroit Surgical LLC’s devices?

Adroit Surgical LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers and regulatory bodies, particularly for Class I devices like their rigid intubation laryngoscopes.

How are Adroit Surgical LLC’s devices classified under FDA regulations?

Adroit Surgical LLC’s rigid intubation laryngoscopes, such as the Vie Scope and Bebe Vie, are classified as Class I devices under FDA regulations. This classification is typically assigned to low-risk medical devices that pose minimal potential harm to patients, though individual devices must still meet regulatory requirements for authorization.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
10001 , Broadway Extension Suite A, Oklahoma City, Oklahoma, United States
LinkedIn
—
Phone
+1 425 577 2713
PRRC Contact
Paul Hagen
EUDAMED SRN
US-MF-000057886
FDA FEI Number
—
DUNS Number
—

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Vie Scope VS-103
FDA UDI
Class IActive
Bebe Vie BB-111
FDA UDI
Class IActive

Related Companies

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