Illusion Plus International

FDA UDI

Class I (US FDA UDI)

by Ortho Organizers, Inc.

Identity

Trade Name: ILLUSION PLUS INTERNATIONAL FDA UDI
Generic Name: Orthodontic bracket, ceramic FDA UDI
Device Name: Illusion Plus™ International .022 UR 4/5 HK -7T 0A 0O FDA UDI
Model / Reference: 708-357HK-10 FDA UDI
Description: Illusion Plus™ International .022 UR 4/5 HK -7T 0A 0O FDA UDI

Identifiers

Primary DI / UDI-DI: 00190707014186 FDA UDI
FDA Product Code: EJF FDA UDI
GMDN Term: Orthodontic bracket, ceramic FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.5410 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Orthodontic bracket, ceramic

Illusion Plus International by Ortho Organizers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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EXPERIENCE® — GC Orthodontics America Inc. · Class II
APC™ PLUS Clarity™ SL — 3M UNITEK CORPORATION · Class II
ClearVu Mini Readi-Base Bracket — TP ORTHODONTICS, INC. · Class II

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: Ortho Organizers, Inc.

Sources (1)

FDA UDI 0952603f-dbee-4934-8e10-2830ee624def 33 fields · synced Jun 9, 2026