FDA Device Establishments · JSON-LD · Markdown

SPINALIGHT INC

FEI 3006315109 · Manufacture Medical Device · Status: Active

FEI Number3006315109
Owner / OperatorSpinalight Inc (#9102583)
Address2201 62ND AVENUE NORTH, St Petersburg, FL, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LXM
Proprietary namesAtlas Percussion Adjusting Instrument

External sources

Source: openFDA. Public-domain (CC0).