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E1 Handpiece, LT

FDA UDI

Class II (US FDA UDI)

by Light Instruments

Identity

Trade Name
E1 Handpiece, LT FDA UDI
Generic Name
Dental solid-state laser system FDA UDI
Device Name
Handpiece for the LightTouch system. FDA UDI
Model / Reference
AS78251 FDA UDI
Description
Handpiece for the LightTouch system. FDA UDI

Identifiers

Catalog Number
AS78251 FDA UDI
Primary DI / UDI-DI
07290016784107 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental solid-state laser system

E1 Handpiece, LT 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 e14934e1-925b-4a92-836b-39a2fcfbaabc 36 fields · synced May 30, 2026