← Back to catalogue

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 adaptor, single-use FDA UDI
Device Name
CUSA Clarity 23kHz Expanded CEM Nosecone (5 Pack) FDA UDI
Model / Reference
C7523X FDA UDI
Description
CUSA Clarity 23kHz Expanded CEM Nosecone (5 Pack) FDA UDI

Identifiers

Catalog Number
C7523X FDA UDI
Primary DI / UDI-DI
10381780536383 FDA UDI
510(k) Number
K230427 FDA UDI
FDA Product Code
LFL FDA UDI
LBK FDA UDI
GMDN Term
Ultrasonic surgical system adaptor, single-use FDA UDI

Classification

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

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ultrasonic surgical system adaptor, single-use

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 adaptor, single-use.

Cleared under the same submission

K230427 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Integra Lifesciences (ireland) Limited

Sources (1)

  • FDA UDI 7fe7d691-2450-47b5-8d2e-c60d1c6e937d 37 fields · synced May 30, 2026