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Symmetry Raney

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Raney FDA UDI
Generic Name
General skin wound clip FDA UDI
Device Name
Symmetry® Clip, Raney Scalp, (12/unit) FDA UDI
Model / Reference
57-8501 FDA UDI
Description
Symmetry® Clip, Raney Scalp, (12/unit) FDA UDI

Identifiers

Catalog Number
57-8501 FDA UDI
Primary DI / UDI-DI
00887482192641 FDA UDI
510(k) Number
K033660 FDA UDI
FDA Product Code
HBO FDA UDI
GMDN Term
General skin wound clip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4150 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

No

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: General skin wound clip

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

Similar devices

Also classified as General skin wound clip.

Cleared under the same submission

K033660 also covers:

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 c0886420-fc0e-4135-8dd0-3a841f0ac767 36 fields · synced May 30, 2026