← Back to catalogue

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
Anatomical Molar Bands, Lower Left 2nd Molars, Size 33 FDA UDI
Model / Reference
774-330 FDA UDI
Description
Anatomical Molar Bands, Lower Left 2nd Molars, Size 33 FDA UDI

Identifiers

Catalog Number
774-330 FDA UDI
Primary DI / UDI-DI
00843471188880 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Young Innovations, Inc.

Sources (1)

  • FDA UDI 72bc4e93-6c0f-4d5c-9a2a-f85fc8151b5f 35 fields · synced Jun 6, 2026