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Symmetry Joseph

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Joseph FDA UDI
Generic Name
Soft-tissue surgical hook, reusable FDA UDI
Device Name
Symmetry® Hook, Joseph Skin, Single-Prong, 6.0 mm, 6 1/4 in, 158 mm FDA UDI
Model / Reference
20-5001 FDA UDI
Description
Symmetry® Hook, Joseph Skin, Single-Prong, 6.0 mm, 6 1/4 in, 158 mm FDA UDI

Identifiers

Catalog Number
20-5001 FDA UDI
Primary DI / UDI-DI
00887482046883 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Soft-tissue surgical hook, 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 — 6 Millimeter FDA UDI
Length — 6.25 Inch FDA UDI

Category: Soft-tissue surgical hook, reusable

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

Similar devices

Also classified as Soft-tissue surgical hook, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8bcb1ca3-1d33-4832-a22a-5600d72d881e 36 fields · synced May 31, 2026