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Myerson db plus

FDA UDI

Class II (US FDA UDI)

by The Myerson Company Limited

Identity

Trade Name
Myerson db plus FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
30° Posterior shade C1, mould L32, U FDA UDI
Model / Reference
T38C1U0L32 FDA UDI
Description
30° Posterior shade C1, mould L32, U FDA UDI

Identifiers

Primary DI / UDI-DI
00842326142879 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

Myerson db plus 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

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Manufacturer

Sources (1)

  • FDA UDI c9e8ad61-1a7e-46d9-bb82-3c10af210da1 35 fields · synced Jun 8, 2026