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Data / Medical devices / United States / Stealth Products

Stealth Products: FDA-registered device maker in Burnet, TX, United States, 2 510(k) clearances

Stealth Products is registered with the FDA (registration 3004473024) in Burnet, TX, United States. It lists 21 device types. The FDA files 2 510(k) clearances under its listings, the newest dated August 12, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004473024
Address
104 John Kelly DR, Burnet, TX, United States, 78611
Owner or operator
PRIDE MOBILITY PRODUCTS CORP. (2523375)
Roles
Manufacturer
First device listed
June 23, 1988
Registered through
2026
Brand names listed
ACCESSORIES, WHEELCHAIR, ARMBOARD, WHEELCHAIR, ARMREST, WHEELCHAIR, BELT, WHEELCHAIR, BOARD, LAP, WHEELCHAIR, BOARD, SCOOTER, PRONE, BRAKE, EXTENSION, WHEELCHAIR, CHAIR, WITH CASTERS 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
August 12, 2011K111739KIDS ROCK 3 CHAIRIORSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov
October 21, 2004K042444LITESTREAM 500EIORSubstantially EquivalentPride Mobility Products Corp.accessdata.fda.gov

Compare with other makers

Updated August 12, 2011. 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.