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The Orthodontic Store

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
The Orthodontic Store FDA UDI
Generic Name
Wire/ligature passer, reusable FDA UDI
Device Name
Ligature Director/Double End FDA UDI
Model / Reference
187-720 FDA UDI
Description
Ligature Director/Double End FDA UDI

Identifiers

Catalog Number
187-720 FDA UDI
Primary DI / UDI-DI
00843471101223 FDA UDI
FDA Product Code
ECP FDA UDI
GMDN Term
Wire/ligature passer, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Wire/ligature passer, reusableOrthodontic ligature director

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

Similar devices

Also classified as Orthodontic ligature director.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1bc87645-8ba0-45ee-be0d-a576bb331e26 35 fields · synced Jun 6, 2026