← Back to catalogue

Kenson

FDA UDI

Class II (US FDA UDI)

by The Myerson Company Limited

Identity

Trade Name
Kenson FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
Anterior shade C2, mould T6, U FDA UDI
Model / Reference
T10C2U00T6 FDA UDI
Description
Anterior shade C2, mould T6, U FDA UDI

Identifiers

Primary DI / UDI-DI
00842326115019 FDA UDI
510(k) Number
K924526 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 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

No

FDA UDI

Category: Resin artificial teeth

Kenson by The Myerson Company Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resin artificial teeth.

Cleared under the same submission

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

Sources (1)

  • FDA UDI d37efe3a-5ec2-484b-b0d0-131444cb5227 35 fields · synced May 31, 2026