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Data / Medical devices / United States / DPM Usa Corp.

DPM Usa Corp.: FDA-registered device maker in Doral, FL, United States, 1 510(k) clearance

DPM Usa Corp. is registered with the FDA (registration 1063774) in Doral, FL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 27, 2009. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1063774
FEI number
3001779742
Address
1460 N.W. 107TH Ave., Ste. G, Doral, FL, United States, 33172
Owner or operator
DPM USA CORP. (9008401)
Roles
Manufacturer
First device listed
December 16, 2009
Registered through
2026
Brand names listed
Switch E, Tubinetta Fit Lux, Tubinetta Ultra, Switch E, Bogotta Light Plus, Bogota Stilla Prime

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
October 27, 2009K090055LOW & HIGH SPEED KITEFASubstantially EquivalentDpm USA Corp.accessdata.fda.gov

Compare with other makers

Updated October 27, 2009. 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.