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Symmetry House

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry House FDA UDI
Generic Name
Tympanotomy knife, reusable FDA UDI
Device Name
Symmetry® Knife, House Tympanoplasty, 7.0mm Curved Blade, 6 1/2 in FDA UDI
Model / Reference
61-0395 FDA UDI
Description
Symmetry® Knife, House Tympanoplasty, 7.0mm Curved Blade, 6 1/2 in FDA UDI

Identifiers

Catalog Number
61-0395 FDA UDI
Primary DI / UDI-DI
00887482114025 FDA UDI
FDA Product Code
KTG FDA UDI
GMDN Term
Tympanotomy knife, reusable 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

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
Width — 7 Millimeter FDA UDI
Length — 6.5 Inch FDA UDI

Category: Tympanotomy knife, reusable

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

Similar devices

Also classified as Tympanotomy knife, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI 93c2b5e7-09d4-4556-a082-9f2b1075b188 36 fields · synced Jun 1, 2026