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Kenson

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref T10A1L0052

by The Myerson Company Limited

Identity

Trade Name
Kenson EUDAMEDFDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
Preformed Artificial Teeth EUDAMED
Anterior shade A1, mould 52, L FDA UDI
Model / Reference
T10A1L0052 EUDAMEDFDA UDI
Description
Anterior shade A1, mould 52, L FDA UDI

Identifiers

Primary DI / UDI-DI
00842326112414 EUDAMEDFDA UDI
Basic UDI-DI
08423261TeethXK EUDAMED
510(k) Number
K924526 FDA UDI
FDA Product Code
ELM FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3590 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 32fbd213-d703-495f-acf2-13775f0725f6 35 fields · synced Oct 6, 2026
  • EUDAMED ba11cd2b-f105-4f71-8aec-89e5342021e0 61 fields · synced Aug 1, 2026