Dexcom
Sistemas de monitoramento contínuo de glicose e sensores de diabetes.
A Dexcom fabrica sistemas de monitoramento contínuo de glicose e sensores de diabetes em suas operações em San Diego. A empresa fornece sistemas de saúde, laboratórios, parceiros OEM ou clientes de exportação regulamentados em seus principais mercados listados.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- San Diego, United States
- Founded
- 1999
- Website
- dexcom.com
- Categories
- Suprimentos médicos e de saúde, Wearables e dispositivos pessoais
- Markets
- Estados Unidos, Alemanha, Reino Unido, Canadá
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
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-07 US EPA Facility Registry Service (national combined file)
- lei-lapsed (amber), checked 2026-08-03 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- customer-reviews (amber), checked 2026-08-08 Sitejabber
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- fda-registered (green), checked 2026-08-08 FDA
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality IAF CertSearch
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)