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CUSA® Clarity

FDA UDI

Class U (US FDA UDI)

by Integra Lifesciences (ireland) Limited

Identity

Trade Name
CUSA® Clarity FDA UDI
Generic Name
Ultrasonic surgical system torque wrench, reusable FDA UDI
Device Name
CUSA® Clarity 23kHz Torque Base FDA UDI
Model / Reference
C7623 FDA UDI
Description
CUSA® Clarity 23kHz Torque Base FDA UDI

Identifiers

Catalog Number
C7623 FDA UDI
Primary DI / UDI-DI
10381780428251 FDA UDI
FDA Product Code
LBK FDA UDI
LFL FDA UDI
GMDN Term
Ultrasonic surgical system torque wrench, reusable FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ultrasonic surgical system torque wrench, reusable

CUSA® Clarity by Integra Lifesciences (ireland) Limited — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic surgical system torque wrench, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Lifesciences (ireland) Limited

Sources (1)

  • FDA UDI c99edc66-6baf-4231-b358-8fe42267e3a5 36 fields · synced May 30, 2026