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Orthoquest

FDA UDI

Class II (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Orthoquest FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
Peppermint Alginate Flavor FDA UDI
Model / Reference
K0139 FDA UDI
Description
Peppermint Alginate Flavor FDA UDI

Identifiers

Catalog Number
K0139 FDA UDI
Primary DI / UDI-DI
00840326406595 FDA UDI
510(k) Number
K940120 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Alginate dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

No

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

Category: Alginate dental impression material

A comprehensive dental impression material for creating accurate and precise oral impressions. This device is used in dentistry to capture detailed information about a patient's teeth, gums, and other oral anatomy.

Similar devices

Also classified as Alginate dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1efc3b41-3f8d-41fb-b18b-0fd648640ce8 36 fields · synced Jun 24, 2026