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Symmetry Karlin™ XL Magnum

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Karlin™ XL Magnum FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
Symmetry® Karlin Curette, Xl Magnum Cup, Forward Angle, 9 mm Tip Size, 13 1/4 in FDA UDI
Model / Reference
46-3232 FDA UDI
Description
Symmetry® Karlin Curette, Xl Magnum Cup, Forward Angle, 9 mm Tip Size, 13 1/4 in FDA UDI

Identifiers

Catalog Number
46-3232 FDA UDI
Primary DI / UDI-DI
00887482015322 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Bone curette, reusable 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

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 — 9 Millimeter FDA UDI
Length — 13.25 Inch FDA UDI

Category: Bone curette, reusable

Symmetry Karlin™ XL Magnum by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a912a6f7-fb21-42a8-b6d3-267079efa5e7 36 fields · synced May 30, 2026