Skip to the page

Data / Medical devices / United States / Intercare DX, Inc.

Intercare DX, Inc.: FDA-registered device maker in Torrance, CA, United States, 1 510(k) clearance

Intercare DX, Inc. is registered with the FDA (registration 3005735282) in Torrance, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 23, 2002. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3005735282
Address
20280 S Vermont Ave Ste 215, Torrance, CA, United States, 90502
Owner or operator
MERIDIAN HEALTH SYSTEMS, P.C. (9084208)
Roles
Manufacturer, Specification developer
First device listed
March 13, 2006
Registered through
2026
Brand names listed
InterCare Vascular Diagnostic Center, VASOCOR(TM) VASCULAR DIA

Devices it lists

DeviceProduct codeClassRoleSource
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Manufacturer, Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 23, 2002K011625VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)DXNSubstantially EquivalentVasocor, Inc.accessdata.fda.gov

Compare with other makers

Updated January 23, 2002. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.