← Back to catalogue

SmartLite® Pro Modular LED Curing Light

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
SmartLite® Pro Modular LED Curing Light FDA UDI
Generic Name
Dental/surgical polymerization lamp FDA UDI
Device Name
SmartLite® Pro O-Rings Refill FDA UDI
Model / Reference
644408 FDA UDI
Description
SmartLite® Pro O-Rings Refill FDA UDI

Identifiers

Catalog Number
644408 FDA UDI
Primary DI / UDI-DI
D0026444081 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental/surgical polymerization lamp

SmartLite® Pro Modular LED Curing Light by Dentsply International — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 414660c5-da86-4aaf-bf7e-03c988f1533c 36 fields · synced Jun 6, 2026