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Data / Medical devices / United States / Techtrade LLC

Techtrade LLC: FDA-registered device maker in Orlando, FL, United States, 1 510(k) clearance

Techtrade LLC is registered with the FDA (registration 3005346101) in Orlando, FL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 17, 2004. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3005346101
Address
6900 Tavistock Lakes Blvd. Ste 400, Orlando, FL, United States, 32827
Owner or operator
TECHTRADE LLC (10029022)
Roles
Manufacturer, Specification developer
First device listed
March 30, 2009
Registered through
2026
Brand names listed
Ready-Heat Blankets

Devices it lists

DeviceProduct codeClassRoleSource
Bedding, Disposable, MedicalKME1Manufacturer, Specification developeraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Manufacturer, 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
September 17, 2004K042145READY-HEAT BLANKETKMESubstantially EquivalentTechtrade, LLCaccessdata.fda.gov

Compare with other makers

Updated September 17, 2004. 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.