g Source

FDA UDI

Class I (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name: g Source FDA UDI
Generic Name: Manual orthopaedic bender, reusable FDA UDI
Device Name: K-Wire and Plate Bender 5 1/2", max cap 1.6mm [.062"] FDA UDI
Model / Reference: gS 82.1020 FDA UDI
Description: K-Wire and Plate Bender 5 1/2", max cap 1.6mm [.062"] FDA UDI

Identifiers

Catalog Number: gS 82.1020 FDA UDI
Primary DI / UDI-DI: 00840314243423 FDA UDI
FDA Product Code: JEX FDA UDI
GMDN Term: Manual orthopaedic bender, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Manual orthopaedic bender, reusable

g Source by Gsource, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Gsource, Llc.

Sources (1)

FDA UDI 1d05bdbb-e060-48b0-a0a4-8dcb419b216c 34 fields · synced May 30, 2026