Symmetry Joseph

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Joseph FDA UDI
Generic Name: Nasal knife FDA UDI
Device Name: Symmetry® Knife, Joseph Nasal, Straight, 25 mm Blade Length, 6 in FDA UDI
Model / Reference: 63-0818 FDA UDI
Description: Symmetry® Knife, Joseph Nasal, Straight, 25 mm Blade Length, 6 in FDA UDI

Identifiers

Catalog Number: 63-0818 FDA UDI
Primary DI / UDI-DI: 00887482117873 FDA UDI
FDA Product Code: KAS FDA UDI
GMDN Term: Nasal knife FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 6 Inch FDA UDI

Category: Nasal knife

Symmetry Joseph by Symmetry Surgical 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: Symmetry Surgical Inc.

Sources (1)

FDA UDI afaba117-a56a-4088-aa51-d8e34f93686e 36 fields · synced Jun 6, 2026