Symmetry Hardy

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Hardy FDA UDI
Generic Name: General/plastic surgery mirror FDA UDI
Device Name: Symmetry® Mirror, Hardy, 5 mm FDA UDI
Model / Reference: 80-1366 FDA UDI
Description: Symmetry® Mirror, Hardy, 5 mm FDA UDI

Identifiers

Catalog Number: 80-1366 FDA UDI
Primary DI / UDI-DI: 00887482030806 FDA UDI
FDA Product Code: GZX FDA UDI
GMDN Term: General/plastic surgery mirror FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4525 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: Width — 5 Millimeter FDA UDI

Category: General/plastic surgery mirror

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

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MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
Mirror, round, polished — Spiggle & Theis Medizintechnik GmbH · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Atticus mirror — Spiggle & Theis Medizintechnik GmbH · Class I
ProneView — DUPACO, 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: Symmetry Surgical Inc.

Sources (1)

FDA UDI ce615614-3af0-4f7d-b597-d013ceafa2e8 36 fields · synced May 30, 2026