Symmetry KERRISON

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry KERRISON FDA UDI
Generic Name: Spinal rongeur FDA UDI
Device Name: Symmetry® Kerrison Rongeur; Lumbar; 90° Up; 3.0 mm; 8 in FDA UDI
Model / Reference: 53-1415 FDA UDI
Description: Symmetry® Kerrison Rongeur; Lumbar; 90° Up; 3.0 mm; 8 in FDA UDI

Identifiers

Catalog Number: 53-1415 FDA UDI
Primary DI / UDI-DI: 00887482022757 FDA UDI
FDA Product Code: HAE FDA UDI
GMDN Term: Spinal rongeur FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4840 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: Length — 8 Inch FDA UDI
Width — 3 Millimeter FDA UDI
Angle — 90 degree FDA UDI

Category: Spinal rongeur

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

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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 II	Pending data

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Manufacturer

Manufacturer: Symmetry Surgical Inc.

Sources (1)

FDA UDI 181e6614-9f76-48e8-85ed-f2c470c3a42a 36 fields · synced Jun 8, 2026