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Ophthalmic Forceps

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Ophthalmic Forceps FDA UDI
Generic Name
Ophthalmic implant handling forceps, reusable FDA UDI
Device Name
KAMRA INLAY FORCEPS FDA UDI
Model / Reference
K5-8510 FDA UDI
Description
KAMRA INLAY FORCEPS FDA UDI

Identifiers

Catalog Number
K5-8510 FDA UDI
Primary DI / UDI-DI
00841668107782 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic implant handling forceps, 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic implant handling forceps, reusable

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

Similar devices

Also classified as Ophthalmic implant handling forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katena Products, Inc.

Sources (1)

  • FDA UDI f7626050-313e-4580-ad45-a3e8ab1f605c 35 fields · synced Jun 12, 2026