{"@context":{"@vocab":"https://schema.org/","dcterms":"http://purl.org/dc/terms/"},"@type":"Organization","@id":"https://api.morvs.ai/medical-device-mfr/3000206450#org","identifier":[{"@type":"PropertyValue","propertyID":"FDA Establishment Identifier (FEI)","value":"3000206450"},{"@type":"PropertyValue","propertyID":"FDA Owner/Operator Number","value":"9089779"}],"name":"TYTEX, INC.","legalName":"TYTEX, INC.","parentOrganization":{"@type":"Organization","name":"TYTEX Slovakia SRO","identifier":"9089779"},"address":{"@type":"PostalAddress","streetAddress":"24 Corliss Street, Unit 40458","addressLocality":"Providence","addressRegion":"RI","postalCode":null,"addressCountry":"US"},"additionalType":["Complaint File Establishment per 21 CFR 820.198"],"additionalProperty":[{"@type":"PropertyValue","propertyID":"FDA Product Codes","value":"NNW"},{"@type":"PropertyValue","propertyID":"Registration expiry year","value":"2026"}],"sameAs":["https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3000206450"],"isAccessibleForFree":true,"license":"https://creativecommons.org/publicdomain/zero/1.0/","_source":{"data_provider":"AI Analytics","brand_name":"MORVS","brand_url":"https://morvs.ai/","data_provider_url":"https://api.morvs.ai","license":"https://creativecommons.org/publicdomain/zero/1.0/","primary_source":"https://open.fda.gov/apis/device/registrationlisting/","generated_at":"2026-11-01T13:08:56.244Z"}}