Qualified source record ยท not independently verified
NEOORTHO PRODUTOS ORTOPEDICOS S/A is listed in FDA device registration data in Curitiba Parana, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
S.I.N. Implant System Ltda is listed in FDA device registration data in SAO PAULO, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
SYSMEX DO BRASIL IND E COM LTDA is listed in FDA device registration data in Sao Jose dos Pinhais Parana, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
TDV DENTAL LTDA is listed in FDA device registration data in POMERODE Santa Catarina, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
Trinity Biotech do Brasil is listed in FDA device registration data in Extrema Minas Gerais, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
ULTIMATE DO BRASIL IMPORTACAO E EXPORTACAO LTDA. is listed in FDA device registration data in SAO JOSE DOS CAMPOS Sao Paulo, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
UNIDADE DE ESTERILIZACAO COTIA LTDA. is listed in FDA device registration data in Cotia Sao Paulo, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Qualified source record ยท not independently verified
VISIO INDUSTRIA E COMERCIO DE EQUIPAMENTOS LTDA is listed in FDA device registration data in Sao Paulo, BR with the establishment role โManufacture Medical Device for Another Party (Contract Manufacturer).โ This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
Profiles identify their evidence level. A qualified source record is not an independently verified supplier, certification, capacity statement or recommendation. How we research suppliers