XL Cone

GUDID 00854103007318

BDA Attachment XL Cone

LITECURE LLC

Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous Musculoskeletal/physical therapy laser beam guide tip, transcutaneous
Primary Device ID00854103007318
NIH Device Record Key43fccabf-713d-4182-a8a2-ec9f757a1ba4
Commercial Distribution StatusIn Commercial Distribution
Brand NameXL Cone
Version Model NumberPRD-000644-000
Company DUNS858768943
Company NameLITECURE LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100854103007318 [Primary]

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-31
Device Publish Date2022-08-23

On-Brand Devices [XL Cone]

00854103007240BDA Attachment XL Cone
00854103007318BDA Attachment XL Cone

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