Dental All Co., Ltd.
Il principale distributore di forniture dentistiche della Thailandia con 20 anni al servizio degli studi dentistici
Dental All è una filiale di Dental Vision, quotata alla Borsa della Thailandia, che opera da oltre 20 anni con un team di oltre 90 addetti alle vendite e all'assistenza. L'azienda distribuisce forniture dentistiche, poltrone, attrezzature e materiali di consumo a cliniche e ospedali in tutta la Thailandia.
- 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
- Forniture e attrezzature dentali
- Markets
- Thailandia
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)