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Symmetry Ostium

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Ostium FDA UDI
Generic Name
Mastoid gauge FDA UDI
Device Name
Symmetry® Seeker, Ostium, w/Double-Ended Ball Tips Maxillary Sinus FDA UDI
Model / Reference
63-8825 FDA UDI
Description
Symmetry® Seeker, Ostium, w/Double-Ended Ball Tips Maxillary Sinus FDA UDI

Identifiers

Catalog Number
63-8825 FDA UDI
Primary DI / UDI-DI
00887482119389 FDA UDI
FDA Product Code
KAK FDA UDI
GMDN Term
Mastoid gauge 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

Category: Mastoid gauge

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

Similar devices

Also classified as Mastoid gauge.

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 e7e042b5-7aeb-4b15-81e6-0c9662f38aab 35 fields · synced May 30, 2026