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TIP for LITETOUCH

FDA UDI

Class II (US FDA UDI)

by Light Instruments

Identity

Trade Name
TIP for LITETOUCH FDA UDI
Generic Name
Dental solid-state laser system FDA UDI
Device Name
Package of 5 reusable tips for the LiteTouch system. FDA UDI
Model / Reference
D-1.0mm L-17mm FDA UDI
Description
Package of 5 reusable tips for the LiteTouch system. FDA UDI

Identifiers

Catalog Number
AS70682 FDA UDI
Primary DI / UDI-DI
07290016784367 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 1.0 Millimeter FDA UDI
Length — 17 Millimeter FDA UDI

Category: Dental solid-state laser system

TIP for LITETOUCH 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 d5c6eec4-9d9e-48af-91ac-577d472ae7a6 37 fields · synced May 30, 2026