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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 12, 2011 | K111739 | KIDS ROCK 3 CHAIR | IOR | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| October 21, 2004 | K042444 | LITESTREAM 500E | IOR | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Mechanical
- All makers of Restraint, Wheelchair, Non-Protective
- All makers of Footrest, Wheelchair
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- All makers of Cuff, Pusher, Wheelchair
- All makers of Belt, Wheelchair
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.