Dental All Co., Ltd.
الموزع الرائد لمستلزمات طب الأسنان في تايلاند مع 20 عامًا في خدمة ممارسات طب الأسنان
Dental All هي شركة تابعة لشركة Dental Vision، المدرجة في بورصة تايلاند، وتعمل منذ أكثر من 20 عامًا مع فريق يضم أكثر من 90 موظفًا للمبيعات والخدمة. تقوم الشركة بتوزيع مستلزمات طب الأسنان والكراسي والمعدات والمواد الاستهلاكية على العيادات والمستشفيات في جميع أنحاء تايلاند.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Bangkok, Thailand
- Founded
- 2006
- Website
- https://dentalall.com
- Categories
- مستلزمات ومعدات طب الأسنان
- Markets
- تايلاند
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
- domain-registered (green), checked 2026-08-08 Domain registry record
- registry-activity (green), checked 2026-08-15 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- financials-published (green), effective since 2025-12-31 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- registry-id-verified (green), checked 2026-08-20 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- lei-lapsed (amber), checked 2026-08-08 GLEIF
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- debarment-clear (green), checked 2026-08-08 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)