Dexcom
أنظمة المراقبة المستمرة للجلوكوز وحساسات مرض السكري.
تقوم Dexcom بتصنيع أنظمة المراقبة المستمرة للجلوكوز وأجهزة استشعار مرض السكري من عملياتها في سان دييغو. توفر الشركة أنظمة الرعاية الصحية والمختبرات وشركاء تصنيع المعدات الأصلية أو عملاء التصدير الخاضعين للتنظيم عبر أسواقها الرئيسية المدرجة.
- 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
- اللوازم الطبية والرعاية الصحية, الأجهزة القابلة للارتداء والأجهزة الشخصية
- Markets
- الولايات المتحدة, ألمانيا, المملكة المتحدة, كندا
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)