LESSpine Innovations Malleable Illuminator 11-07032

GUDID 00812432022464

LUMITEX, INC.

Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light source Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light Open surgical site internal light
Primary Device ID00812432022464
NIH Device Record Keyfc220b30-9968-4a00-bf07-119389906b18
Commercial Distribution StatusIn Commercial Distribution
Brand NameLESSpine Innovations Malleable Illuminator
Version Model Number010104
Catalog Number11-07032
Company DUNS108631797
Company NameLUMITEX, INC.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812432022464 [Primary]

FDA Product Code

FDGRetractor, Fiberoptic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-29
Device Publish Date2021-03-19

Devices Manufactured by LUMITEX, INC.

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00812432022396 - Spineart Wolf Cable Adaptor2023-08-21
00812432022921 - Spineart Olympus Cable Adaptor2023-08-21
00810025485344 - MiRus Bifurcated Illuminator2023-08-21
00812432021559 - Spineart Storz Cable Adaptor2023-08-21
00812432021689 - Lumitex 4mm Universal Fiber Optic Cable2023-08-21
00812432021696 - Lumitex 3.5mm Fiber Optic Cable2023-08-21
00812432022655 - Orthofix Surgical Illuminator2023-08-21

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