Multi Fa

FDA UDI

Class I (US FDA UDI)

by GC Orthodontics America Inc.

Identity

Trade Name: MULTI FA FDA UDI
Generic Name: Orthodontic spring FDA UDI
Device Name: MULTI FA LONG (LEFT & RIGHT) FDA UDI
Model / Reference: 92-5003-0000 FDA UDI
Description: MULTI FA LONG (LEFT & RIGHT) FDA UDI

Identifiers

Catalog Number: 92-5003-0000 FDA UDI
Primary DI / UDI-DI: D78892500300001 FDA UDI
FDA Product Code: DYJ FDA UDI
GMDN Term: Orthodontic spring 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Orthodontic spring

Multi Fa by GC Orthodontics America Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Orthodontic Spring — DENTOS Inc. · Class I
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Begg Spring-Pin — TP ORTHODONTICS, INC. · Class I
Ortho Organizers — Ortho Organizers, Inc. · Class I

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: GC Orthodontics America Inc.

Sources (1)

FDA UDI 6e1b417c-aca0-4ec6-9a60-0ee552ab8c8a 35 fields · synced Jun 8, 2026