Dental All Co., Ltd.
20 yıldır diş hekimliği muayenehanelerine hizmet veren Tayland'ın önde gelen diş malzemeleri distribütörü
Dental All, Tayland Menkul Kıymetler Borsası'nda işlem gören Dental Vision'ın bir yan kuruluşudur ve 90'dan fazla satış ve servis personelinden oluşan bir ekiple 20 yılı aşkın süredir faaliyet göstermektedir. Şirket, Tayland genelindeki kliniklere ve hastanelere dişçilik malzemeleri, sandalyeler, ekipman ve sarf malzemeleri dağıtıyor.
- 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
- Diş Malzemeleri ve Ekipmanları
- Markets
- Tayland
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)