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Dentronix

FDA UDI

Class II (US FDA UDI)

by Dentronix, Inc.

Identity

Trade Name
Dentronix FDA UDI
Generic Name
Dental/surgical polymerization lamp FDA UDI
Device Name
Dentronix LED 3000 Plug Type A FDA UDI
Model / Reference
60013947 FDA UDI
Description
Dentronix LED 3000 Plug Type A FDA UDI

Identifiers

Primary DI / UDI-DI
D661600139470 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

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental/surgical polymerization lamp

Dentronix by Dentronix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental/surgical polymerization lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentronix, Inc.

Sources (1)

  • FDA UDI 0243ca94-212f-4d3b-b1c2-0dd6f3547824 34 fields · synced May 30, 2026