Data / Medical devices / United States / Merits Health Products, Inc.
Merits Health Products, Inc.: FDA-registered device maker in Las Vegas, NV, United States, 13 510(k) clearances
Merits Health Products, Inc. is registered with the FDA (registration 3030822491) in Las Vegas, NV, United States. It lists 6 device types. The FDA files 13 510(k) clearances under its listings, the newest dated July 10, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030822491
- Address
- 5551 E North Belt Rd Ste 189, Las Vegas, NV, United States, 89115
- Owner or operator
- Merits Health Products, Inc. (10095814)
- Roles
- Contract manufacturer, Repackager or relabeler
- First device listed
- May 4, 2026
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cushion, Wheelchair | IMP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Powered Stairway Chair Lift | PCD | 2 | Repackager or relabeler | accessdata.fda.gov |
| Vehicle, Motorized 3-Wheeled | INI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Contract manufacturer, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| July 10, 2019 | K182471 | Scooter | INI | Substantially Equivalent | Tianjin Kepler Vehicle Industry Co. , Ltd. | accessdata.fda.gov |
| May 1, 2015 | K142162 | MERITS TRANSFORMER POWER SCOOTER, S941 | INI | Substantially Equivalent | Merits Health Products Co., Ltd. | accessdata.fda.gov |
| January 9, 2013 | K122357 | MERITS MODEL P322FWD POWERED WHEELCHAIR | ITI | Substantially Equivalent | Merits Health Products Co., Ltd. | accessdata.fda.gov |
| May 8, 2012 | K113577 | MERITS MODEL R SERIES POSITIONING SYSTEM FOR POWERED WHEELCHAIR | ITI | Substantially Equivalent | Merits Health Products Co., Ltd. | accessdata.fda.gov |
| September 18, 2001 | K012802 | MP3CF ELECTRIC WHEELCHAIR | ITI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| August 10, 2001 | K011513 | MP3U, POWER WHEELCHAIR | ITI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| August 6, 2001 | K011751 | TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 3 | INI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| August 3, 2001 | K011753 | TRAVEL EASE ELECTRIC SCOOTER, MODEL PIONEER 4 | INI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| August 3, 2001 | K011687 | MP-3C POWER BASE CHAIR, MODEL MP3C | ITI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| May 9, 2001 | K010380 | MP3HD BIG BOY, POWER WHEELCHAIR | ITI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| November 5, 1999 | K993032 | MODIFICATION TO MP-3 POWER BASE CHAIR | ITI | Substantially Equivalent | Merits Health Products., Inc. | accessdata.fda.gov |
| March 4, 1996 | K952042 | TRAVEL EASE ELECTRIC SCOOTER, MODEL: PIONEER | INI | Substantially Equivalent | Merits Health Products Co., Ltd. | accessdata.fda.gov |
| March 30, 1994 | K933662 | MERITS WHEELCHAIR | ITI | Substantially Equivalent for Some Indications | Merits Health Products., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Powered
- All makers of Vehicle, Motorized 3-Wheeled
- All makers of Powered Stairway Chair Lift
- All makers of Cushion, Wheelchair
- All makers of Accessories, Wheelchair
- All makers of Components, Wheelchair
Updated July 10, 2019. 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.