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LiteTouch Applicator

FDA UDI

Class II (US FDA UDI)

by Light Instruments

Identity

Trade Name
LiteTouch Applicator FDA UDI
Generic Name
Dental solid-state laser system FDA UDI
Device Name
YAG Laser Applicator. LiteTouch Applicator. FDA UDI
Model / Reference
LI-FG0015A FDA UDI
Description
YAG Laser Applicator. LiteTouch Applicator. FDA UDI

Identifiers

Catalog Number
LI-FG0015A FDA UDI
Primary DI / UDI-DI
07290016784022 FDA UDI
510(k) Number
K061966 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dental solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental solid-state laser system

LiteTouch Applicator by Light Instruments — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental solid-state laser system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Light Instruments

Sources (1)

  • FDA UDI 644f6bc5-1703-4f70-ac1e-3d31e9903264 36 fields · synced May 30, 2026