Symmetry House

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry House FDA UDI
Generic Name: General/plastic surgery mirror FDA UDI
Device Name: Symmetry® Mirror, House Middle Ear, Angled 45° on Straight Shaft, 2.5 mm Mirrors, 6 1/2 in FDA UDI
Model / Reference: 61-0390 FDA UDI
Description: Symmetry® Mirror, House Middle Ear, Angled 45° on Straight Shaft, 2.5 mm Mirrors, 6 1/2 in FDA UDI

Identifiers

Catalog Number: 61-0390 FDA UDI
Primary DI / UDI-DI: 00887482113974 FDA UDI
FDA Product Code: FTX FDA UDI
GMDN Term: General/plastic surgery mirror FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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: Angle — 45 degree FDA UDI
Length — 6.5 Inch FDA UDI

Category: General/plastic surgery mirror

Symmetry House 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
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 723076d1-235d-4a44-bfe1-5fb17254cd3e 36 fields · synced Jun 8, 2026