Data / Medical devices / United States / Mega Motion, Inc.
Mega Motion, Inc.: FDA-registered device maker in Duryea, PA, United States, 3 510(k) clearances
Mega Motion, Inc. is registered with the FDA (registration 2531618) in Duryea, PA, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 2, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2531618
- FEI number
- 3002608037
- Address
- 401 York Avenue, Duryea, PA, United States, 18642
- Owner or operator
- PRIDE MOBILITY PRODUCTS CORP. (2523375)
- Roles
- Manufacturer
- First device listed
- April 22, 2008
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Positioning, Electric | INO | 2 | Manufacturer | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 2, 2009 | K091578 | LIFT CHAIR, MODEL T3 | INO | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| April 16, 2007 | K070950 | LIFT CHAIR, MODEL C5 | INO | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
| November 17, 2006 | K063389 | GO GO ELITE TRAVELLER PLUS 4 WHEEL SCOOTER, MODEL SC54 | INI | Substantially Equivalent | Pride Mobility Products Corp. | accessdata.fda.gov |
Compare with other makers
Updated December 2, 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.