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Data / Medical devices / United States / Pedigo Products, Inc.

Pedigo Products, Inc.: FDA-registered device maker in Vancouver, WA, United States, 2 510(k) clearances

Pedigo Products, Inc. is registered with the FDA (registration 2024242) in Vancouver, WA, United States. It lists 8 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 6, 2013. 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
2024242
Address
4000 S.E. Columbia Way, Vancouver, WA, United States, 98661
Owner or operator
PEDIGO PRODUCTS, INC. (2024242)
Roles
Manufacturer, Specification developer
First device listed
December 16, 1992
Registered through
2026
Brand names listed
CDS-3060-DD, CDS-3072-DD, DC250L, DC400L, EC1350BL, EC1540, EC1850BL, EC250L and more

Devices it lists

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
December 6, 2013K132202DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINETLGZSubstantially EquivalentEnthermics Medical Systems, Inc.accessdata.fda.gov
May 7, 2010K091336IVNOW MODULAR FLUID WARMER, 120V, MODEL IVNOW-1, IVNOW-2, IVNOW-3, IVNOW-6, IVNOW MODULAR FLUID WARMER 230VLGZSubstantially EquivalentEnthermics Medical Systems, Inc.accessdata.fda.gov

Compare with other makers

Updated December 6, 2013. 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.