Curette

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name: Curette FDA UDI
Generic Name: Ophthalmic curette, reusable FDA UDI
Device Name: ANIS CAPSULE SCRUBBER DISC FDA UDI
Model / Reference: K3-1111 FDA UDI
Description: ANIS CAPSULE SCRUBBER DISC FDA UDI

Identifiers

Catalog Number: K3-1111 FDA UDI
Primary DI / UDI-DI: 00841668102138 FDA UDI
FDA Product Code: HNZ FDA UDI
GMDN Term: Ophthalmic curette, reusable 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

FDA UDI

Single Use

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

Category: Ophthalmic curette, reusable

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

Similar devices

Also classified as Ophthalmic curette, reusable.

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Ambler Surgical — Ambler Surgical, LLC · Class I
Sklar® — Sklar Corporation · Class I
Curette — Koros USA, Inc. · Class I
ASELTECH — Asel Tibbi Aletler A.S. · Class I
BOSS Instruments — Boss Instruments, Ltd. · Class I
Comfort Plus Curette — Koros USA, Inc. · Class I
MSI Precision Specialty Instruments — Med Saver, Inc. · Class I

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 ee854395-5b2a-4084-bee2-660d2a98a158 35 fields · synced Jun 12, 2026