Mini Master Series

FDA UDI

Class I (US FDA UDI)

by American Orthodontics

Identity

Trade Name: Mini Master Series FDA UDI
Generic Name: Orthodontic bracket, metal FDA UDI
Device Name: DB BKT MINI MS UL CEN 018 T+24 A+3 R=0 FDA UDI
Model / Reference: 310-2002 FDA UDI
Description: DB BKT MINI MS UL CEN 018 T+24 A+3 R=0 FDA UDI

Identifiers

Catalog Number: 310-2002 FDA UDI
Primary DI / UDI-DI: 00190746108396 FDA UDI
FDA Product Code: EJF FDA UDI
GMDN Term: Orthodontic bracket, metal 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

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Orthodontic bracket, metal

Mini Master Series by American Orthodontics — 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: American Orthodontics

Sources (1)

FDA UDI e92cd8ea-32a8-4a37-97cb-8b842c812e34 35 fields · synced Jun 9, 2026