J. Morita Mfg. Corp.
Стоматологические материалы и оборудование, Япония
J. Morita Mfg. Corp. , компания по производству стоматологических принадлежностей и оборудования, базирующаяся в Осаке, Япония.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Osaka, Japan
- Website
- https://www.morita.com/
- Categories
- Стоматологические материалы и оборудование
- Markets
- Япония
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- manufacturing-practice-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- insured-workplace (green), checked 2026-08-23 gBizINFO (Ministry of Economy, Trade and Industry), establishment records from the social insurance system
- domain-registered (green), checked 2026-08-09 Domain registry record
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- registry-id-verified (green), checked 2026-09-22 gBizINFO (Ministry of Economy, Trade and Industry), government-held corporate data
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- fda-registered (green), checked 2026-08-09 FDA
- debarment-clear (green), checked 2026-08-09 OpenSanctions
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)