Data / Medical devices / United States / Avivo Life, LLC
Avivo Life, LLC: FDA-registered device maker in Rockville, MD, United States, 3 510(k) clearances
Avivo Life, LLC is registered with the FDA (registration 3044085583) in Rockville, MD, United States. It lists 12 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 16, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044085583
- Address
- 1395 Piccard Dr Suite 200 - M18, Rockville, MD, United States, 20850
- Owner or operator
- Avivo Life, LLC (10095502)
- Roles
- Complaint file establishment, Repackager or relabeler
- First device listed
- March 20, 2026
- Registered through
- 2026
- Brand names listed
- Avivo Life Cane, Avivo Life Chair with Casters, Avivo Life Commode & Wheelchair Attachments, Avivo Life Crutch, Avivo Life Mechanical Table, Avivo Life Mechanical Walker and Rollator, Avivo Life Recreational Adaptor, Avivo Life Shower Chair and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Adaptor, Recreational | ILT | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Attachment, Commode, Wheelchair | INB | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Cane | IPS | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Chair, Geriatric | FRJ | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Crutch | IPR | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Table, Mechanical | INW | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Tips And Pads, Cane, Crutch And Walker | INP | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| August 16, 2006 | K062218 | JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP | IOR | Substantially Equivalent | Jan Mao Industries Co., Ltd. | accessdata.fda.gov |
| June 29, 2005 | K051482 | JAN MAO WHEELCHAIR, MODEL JMC612-F18EPP | IOR | Substantially Equivalent | Jan Mao Industries Co., Ltd. | accessdata.fda.gov |
| June 29, 2005 | K051481 | JAN MAO WHEELCHAIR, MODEL JMC611-F18EPP | IOR | Substantially Equivalent | Jan Mao Industries Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, Geriatric
- All makers of Tips And Pads, Cane, Crutch And Walker
- All makers of Adaptor, Recreational
- All makers of Crutch
- All makers of Wheelchair, Mechanical
- All makers of Components, Wheelchair
Updated August 16, 2006. 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.