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OraPro

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
OraPro FDA UDI
Generic Name
Orthodontic metal band FDA UDI
Device Name
YS SL MBT 022 LL4 - 5PK FDA UDI
Model / Reference
MSLM22LL4 FDA UDI
Description
YS SL MBT 022 LL4 - 5PK FDA UDI

Identifiers

Catalog Number
MSLM22LL4 FDA UDI
Primary DI / UDI-DI
00840326405260 FDA UDI
FDA Product Code
ECM FDA UDI
GMDN Term
Orthodontic metal band 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

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

Category: Orthodontic metal band

OraPro by Young Innovations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic metal band.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b3da87d-e1b1-4607-8c2d-047244e1436f 35 fields · synced Jun 6, 2026