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Unique Technologies, Inc.

US

Last updated May 24, 2026

What Unique Technologies, Inc. makes

Unique Technologies, Inc. manufactures single-use surgical scalpels, including variants such as the Unique Edge and EDGETEC, designed for precision cutting in medical procedures.

These devices fall under FDA Class I regulation 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 Unique Technologies, Inc. manufacture?

Unique Technologies, Inc. specializes in single-use surgical scalpels. Their product line includes variants like the Unique Edge and EDGETEC, all designed for precise cutting during surgical procedures. These devices are intended for one-time use to reduce infection risks and improve patient safety.

Where is Unique Technologies, Inc. based?

Unique Technologies, Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance and distribution, as it operates within the FDA’s jurisdiction for device authorization.

Which regulatory registries list Unique Technologies, Inc.’s devices?

Unique Technologies, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, clinical, and supply chain purposes, ensuring traceability and compliance with FDA requirements.

How are Unique Technologies, Inc.’s devices classified by the FDA?

All of Unique Technologies, Inc.’s devices fall under FDA Class I classification. This classification applies to low-risk devices that pose minimal potential harm to users, often requiring less stringent regulatory oversight than higher-risk categories.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1(877)991-1110
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
927892380

Catalogue (223)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
Unique Edge 55-1720
FDA UDI
Class IActive
Unique Edge 52-1840-G
FDA UDI
Class IActive
Unique Edge 52-1552
FDA UDI
Class IActive
Unique Edge 58-5702
FDA UDI
Class IActive
Unique Edge 54-1031
FDA UDI
Class IActive
Unique Edge 55-1520
FDA UDI
Class IActive
Unique Edge 52-2241
FDA UDI
Class IActive
Edgetec EDGE4-1.8
FDA UDI
Class IActive
Unique Edge 52-2701
FDA UDI
Class IActive
Unique Edge 51-2531
FDA UDI
Class IActive
Unique Edge 52-2862
FDA UDI
Class IActive
Unique Edge 58-2012
FDA UDI
Class IActive
Unique Edge 51-2061
FDA UDI
Class IActive
Unique Edge 52-2542
FDA UDI
Class IActive
Unique Edge 52-2842
FDA UDI
Class IActive
Unique Edge 58-2008
FDA UDI
Class IActive
Unique Edge 52-2561-G
FDA UDI
Class IActive
Unique Edge 52-3240
FDA UDI
Class IActive
Unique Edge 52-2452
FDA UDI
Class IActive
Unique Edge 52-3050
FDA UDI
Class IActive
Unique Edge 52-2830
FDA UDI
Class IActive
Unique Edge 52-2961
FDA UDI
Class IActive
Sharpoint EDGE 72-2750
FDA UDI
Class IActive

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