FDA Device Establishments · JSON-LD · Markdown

Lumitex Medical Devices, Inc.

FEI 1000122810 · Manufacture Medical Device · Status: Active

FEI Number1000122810
Owner / OperatorLumitex Medical Devices, Inc. (#9000093)
Address6611 W Snowville Rd, Brecksville, OH, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LBI
Regulation § (21 CFR)880.5700
Proprietary namesGiraffe Blue Spot PT Lite

External sources

Source: openFDA. Public-domain (CC0).