Paeon Anterior Cervical Plate System

FDA UDI

Class I (US FDA UDI)

by Aegis Spine, Inc.

Identity

Trade Name: Paeon Anterior Cervical Plate System FDA UDI
Generic Name: Manual orthopaedic bender, reusable FDA UDI
Device Name: Plate Bender FDA UDI
Model / Reference: CP02-0701 FDA UDI
Description: Plate Bender FDA UDI

Identifiers

Catalog Number: CP02-0701 FDA UDI
Primary DI / UDI-DI: 00840273301592 FDA UDI
FDA Product Code: HXW FDA UDI
GMDN Term: Manual orthopaedic bender, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 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

Dry Heat Sterilization FDA UDI

Category: Manual orthopaedic bender, reusable

Paeon Anterior Cervical Plate System by Aegis Spine, Inc. — 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: Aegis Spine, Inc.

Sources (1)

FDA UDI 9d1be909-1484-4e17-82df-7f9a747f7cec 34 fields · synced Jun 8, 2026