Dexcom
Systemy ciągłego monitorowania poziomu glukozy i czujniki cukrzycy.
Dexcom produkuje systemy ciągłego monitorowania poziomu glukozy i czujniki cukrzycy w swoich oddziałach w San Diego. Firma zaopatruje systemy opieki zdrowotnej, laboratoria, partnerów OEM lub regulowanych klientów eksportowych na swoje notowane na rynkach głównych.
- 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
- Artykuły medyczne i związane z opieką zdrowotną, Urządzenia do noszenia i urządzenia osobiste
- Markets
- Stany Zjednoczone, Niemcy, Wielka Brytania, Kanada
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)