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LightForce EXPi

FDA UDI

Class II (US FDA UDI)

by Litecure Llc

Identity

Trade Name
LightForce EXPi FDA UDI
Generic Name
Musculoskeletal/physical therapy laser, professional FDA UDI
Device Name
Mains powered, infrared phototherapy and nail laser phototherapy device emitting up to 25 W at 980/810nm in CW or pulsed modes with a 10" touch screen display. FDA UDI
Model / Reference
LTS-2500 FDA UDI
Description
Mains powered, infrared phototherapy and nail laser phototherapy device emitting up to 25 W at 980/810nm in CW or pulsed modes with a 10" touch screen display. FDA UDI

Identifiers

Primary DI / UDI-DI
00854103007059 FDA UDI
FDA Product Code
PDZ FDA UDI
ILY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
890.5500 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Musculoskeletal/physical therapy laser, professionalNail laser phototherapy unit

LightForce EXPi by Litecure Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nail laser phototherapy unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Litecure Llc

Sources (1)

  • FDA UDI afc8d452-ab5e-42b2-8b32-ccbffe253c20 34 fields · synced Jun 6, 2026