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Ledex

FDA UDI

Class II (US FDA UDI)

by Dentmate Technology Co. , Ltd.

Identity

Trade Name
LEDEX FDA UDI
Generic Name
Dental/surgical polymerization lamp FDA UDI
Device Name
WL-070 Pink (US) FDA UDI
Model / Reference
WL-070 FDA UDI
Description
WL-070 Pink (US) FDA UDI

Identifiers

Primary DI / UDI-DI
04719873920143 FDA UDI
510(k) Number
K082408 FDA UDI
FDA Product Code
EBZ FDA UDI
GMDN Term
Dental/surgical polymerization lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6070 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental/surgical polymerization lamp

Ledex by Dentmate Technology Co. , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/surgical polymerization lamp.

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 9f7d20ea-832b-4a42-9bbf-5f92564cbd1e 34 fields · synced Jun 8, 2026