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Astek

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Astek FDA UDI
Generic Name
Dental impression tray, single-use FDA UDI
Device Name
Transform Tray - Edentulous - Mixed Bag 2 x #7-12 FDA UDI
Model / Reference
118213 FDA UDI
Description
Transform Tray - Edentulous - Mixed Bag 2 x #7-12 FDA UDI

Identifiers

Catalog Number
118213 FDA UDI
Primary DI / UDI-DI
00840326419403 FDA UDI
FDA Product Code
EHY FDA UDI
GMDN Term
Dental impression tray, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6880 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

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: Dental impression tray, single-use

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

Similar devices

Also classified as Dental impression tray, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 38150e45-f750-4097-9eed-fd4db5a249a6 35 fields · synced May 31, 2026