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Symmetry Surgical

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Surgical FDA UDI
Generic Name
Bone hook FDA UDI
Device Name
Symmetry® Hook, Bone, Sharp, Heavy Duty, 30 mm Diamteter, 9 in, 228 mm FDA UDI
Model / Reference
32-3425 FDA UDI
Description
Symmetry® Hook, Bone, Sharp, Heavy Duty, 30 mm Diamteter, 9 in, 228 mm FDA UDI

Identifiers

Catalog Number
32-3425 FDA UDI
Primary DI / UDI-DI
00887482006221 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Bone hook 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
Length — 9 Inch FDA UDI

Category: Bone hook

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

Similar devices

Also classified as Bone hook.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8689c36c-679c-4308-bc2a-790cd3421f8d 36 fields · synced May 31, 2026