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ClearCut®

FDA UDI

Class I (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
ClearCut® FDA UDI
Generic Name
Ophthalmic knife, single-use FDA UDI
Device Name
ClearCut® HP2 Slit Knife Dual Bevel 2.8mm Angled FDA UDI
Model / Reference
8065982865 FDA UDI
Description
ClearCut® HP2 Slit Knife Dual Bevel 2.8mm Angled FDA UDI

Identifiers

Primary DI / UDI-DI
00380659828652 FDA UDI
FDA Product Code
HNN FDA UDI
GMDN Term
Ophthalmic knife, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic knife, single-use

ClearCut® by Alcon Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic knife, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9cdca70f-6367-4303-99db-c7b0926e9a56 34 fields · synced May 30, 2026