Dexcom
连续血糖监测系统和糖尿病传感器。
Dexcom 在其圣地亚哥工厂生产连续血糖监测系统和糖尿病传感器。该公司在其上市主要市场上为医疗保健系统、实验室、OEM 合作伙伴或受监管的出口客户提供服务。
- 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
- 医疗保健用品, 可穿戴设备和个人设备
- Markets
- 美国, 德国, 英国, 加拿大
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)