LightForce PRO

GUDID 00854103007004

Mains powered, infrared phototherapy device emitting up to 9 W at 980 nm. The LightForce PRO (LTC-900) is indicated for emitting energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for temporary relief of minor muscle and joint pain, muscle spasm, pain and stiffness associated with arthritis and promoting. relaxation of the muscle tissue and to temporarily increase local blood circulation. The PRO is a compact, portable medical laser therapy system. The laser light delivery system consists of a flexible optical fiber threaded through a lightweight hand piece. Activation occurs when the operator enables the laser and presses the finger switch. Depending on laser system configuration, the finger switch can function as an on/off switch. A touch-screen display panel allows the operator to adjust or set laser output level. The laser can operate in continuous wave mode or controlled pulse mode.

LITECURE LLC

Musculoskeletal infrared phototherapy unit, non-wearable
Primary Device ID00854103007004
NIH Device Record Keya1b35558-5654-478d-b757-e57b30b9ae80
Commercial Distribution StatusIn Commercial Distribution
Brand NameLightForce PRO
Version Model NumberLTC-900
Company DUNS858768943
Company NameLITECURE LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com
Phone1-877-627-3858
Emailcustomer.service@litecure.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100854103007004 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-06
Device Publish Date2017-02-07

Devices Manufactured by LITECURE LLC

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00854103007318 - XL Cone2022-08-31 BDA Attachment XL Cone
00854103007325 - XL Rolling Pin2022-08-31 BDA Xl Rolling Pin Attachment
00854103007110 - Empower Delivery System2022-07-08 Basic Hand Piece (BHP)_600um Fiber Assy (White)
00854103007134 - Empower IQ Delivery System2022-07-08 Smart Hand Piece (SHP)_800um Fiber Assy v2
00854103007165 - Empower Delivery System2022-07-08 Legacy Hand Piece 800um Fiber Hand Piece w/ Finger Switch, Cool Gray
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