← Back to catalogue

Westcott Tenotomy Scissors 22mm Left

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
WESTCOTT TENOTOMY SCISSORS 22MM LEFT FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Device Name
WESTCOTT TENOTOMY SCISSORS 22MM LEFT FDA UDI
Model / Reference
AE-5501 FDA UDI
Description
WESTCOTT TENOTOMY SCISSORS 22MM LEFT FDA UDI

Identifiers

Catalog Number
AE-5501 FDA UDI
Primary DI / UDI-DI
00841668137086 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, conventional-hinge, 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: Intraocular scissors, conventional-hinge, reusable

Westcott Tenotomy Scissors 22mm Left by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors, conventional-hinge, reusable.

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
Katena Products, Inc.

Sources (1)

  • FDA UDI 54705fe2-5d29-4a11-b517-71c92a1ddec0 35 fields · synced Jun 12, 2026