FDA Device Establishments · JSON-LD · Markdown

Lumitex, Celaya

FEI 3030101746 · Manufacture Medical Device · Status: Active

FEI Number3030101746
Owner / OperatorLumitex Medical Devices, Inc. (#9000093)
AddressCarr. Celaya a Salvatierra Km. 17, Col. Predio Rustico las Palomas Int.1, Celaya Guanajuato, 38150, MX
Mandatory US AgentLUMITEX MD, INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FDG
Regulation § (21 CFR)876.4530
Proprietary namesMedtronic Surgical Illuminator - Tube; LESSpine Malleable Illuminator 4mm MAX Cable Diameter; Spineart Wolf Cable Adapter; Camber Spine MIS Surgical Illuminator 3.75mm MAX Cable Diameter; Globus Medical 4mm Olympus Cable Adapter; Orthofix Surgical Illuminator; Seaspine Wolf Cable Adapter; CoreLink Bifurcated Illuminator 3mm MAX Cable Diameter; Globus Medical MARS Port Illuminator- 19mm 4mm MAX Cable Diameter; K2M Canyon Retractor Systems 20mm

External sources

Source: openFDA. Public-domain (CC0).