Data / Medical devices / United States / Medical Rehab Products, LLC
Medical Rehab Products, LLC: FDA-registered device maker in Watkinsville, GA, United States, 1 510(k) clearance
Medical Rehab Products, LLC is registered with the FDA (registration 3013538349) in Watkinsville, GA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 17, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013538349
- Address
- 1071 Jamestown Blvd Suite 405, Watkinsville, GA, United States, 30677
- Owner or operator
- Medical Rehab Products, LLC (10053431)
- Roles
- Manufacturer
- First device listed
- March 30, 2017
- Registered through
- 2026
- Brand names listed
- Athena Chair, Athena Legrest
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Footrest, Wheelchair | IMM | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| May 17, 2018 | K173360 | Athena 190 | IOR | Substantially Equivalent | Medical Rehab Products, LLC | accessdata.fda.gov |
Compare with other makers
Updated May 17, 2018. 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.