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Orthoquest

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Orthoquest FDA UDI
Generic Name
Orthodontic spring FDA UDI
Device Name
009/010X030 Closcoil Spg 40In FDA UDI
Model / Reference
015-720 FDA UDI
Description
009/010X030 Closcoil Spg 40In FDA UDI

Identifiers

Catalog Number
015-720 FDA UDI
Primary DI / UDI-DI
00843471157442 FDA UDI
FDA Product Code
ECO FDA UDI
GMDN Term
Orthodontic spring 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

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

Orthoquest by Young Innovations, Inc. — 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 0a07a8b3-7815-4eba-abaf-d05d3cf8aa80 36 fields · synced May 30, 2026