← Back to catalogue

Symmetry Fox

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Fox FDA UDI
Generic Name
Ophthalmic soft-tissue surgical forceps probe-tip, reusable FDA UDI
Device Name
Symmetry® Introducer, Fox Sphere, 4 7/8 in FDA UDI
Model / Reference
60-3023 FDA UDI
Description
Symmetry® Introducer, Fox Sphere, 4 7/8 in FDA UDI

Identifiers

Catalog Number
60-3023 FDA UDI
Primary DI / UDI-DI
00887482040010 FDA UDI
FDA Product Code
HNP FDA UDI
GMDN Term
Ophthalmic soft-tissue surgical forceps probe-tip, 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 4.875 Inch FDA UDI

Category: Ophthalmic soft-tissue surgical forceps probe-tip, reusable

Symmetry Fox by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue surgical forceps probe-tip, 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
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI 55b2ee39-e3a8-4b2d-b5d1-48b39034dee9 36 fields · synced May 30, 2026