Symmetry Cohen

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Cohen FDA UDI
Generic Name: Haemorrhoid ligator FDA UDI
Device Name: Symmetry® Acorn; Cohen; Large FDA UDI
Model / Reference: 52-0837 FDA UDI
Description: Symmetry® Acorn; Cohen; Large FDA UDI

Identifiers

Catalog Number: 52-0837 FDA UDI
Primary DI / UDI-DI: 00887482076842 FDA UDI
510(k) Number: K060233 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Haemorrhoid ligator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

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

Category: Haemorrhoid ligator

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

Similar devices

Also classified as Haemorrhoid ligator.

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Sklar® — Sklar Corporation · Class I
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ESI — FTT MEDICAL, INC. · Class II
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II

Cleared under the same submission

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 27d3c324-11aa-4214-b499-fdd461ea2139 36 fields · synced Jun 8, 2026