Ophthalmic Knife

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name: Ophthalmic Knife FDA UDI
Generic Name: Ophthalmic knife, single-use FDA UDI
Device Name: SIDEPORT KNIFE 1MM ANGLED (BX/5) FDA UDI
Model / Reference: K20-2294 FDA UDI
Description: SIDEPORT KNIFE 1MM ANGLED (BX/5) FDA UDI

Identifiers

Catalog Number: K20-2294 FDA UDI
Primary DI / UDI-DI: 00841668113264 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Ophthalmic knife, single-use

Ophthalmic Knife by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Katena Products, Inc.

Sources (1)

FDA UDI 3eef6182-29c8-4269-8e70-e46fbe72c69a 35 fields · synced Jun 12, 2026