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Master Series

FDA UDI

Class I (US FDA UDI)

by American Orthodontics

Identity

Trade Name
Master Series FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
DB BKT MINI MS HGW UL BIC 022 T-6 A=0 R=0 W/HK MES FDA UDI
Model / Reference
310-0115B FDA UDI
Description
DB BKT MINI MS HGW UL BIC 022 T-6 A=0 R=0 W/HK MES FDA UDI

Identifiers

Catalog Number
310-0115B FDA UDI
Primary DI / UDI-DI
00190746095795 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
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Master Series by American Orthodontics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7357a2e8-f124-4c0b-8ca3-ae719dad2442 36 fields · synced Jun 9, 2026