Data / Medical devices / United States / ReliefBand Technologies
ReliefBand Technologies: FDA-registered device maker in Horsham, PA, United States, 4 510(k) clearances
ReliefBand Technologies is registered with the FDA (registration 3006614152) in Horsham, PA, United States. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated August 30, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006614152
- Address
- 300 Welsh Road Building One, Suite 100, Horsham, PA, United States, 19044
- Owner or operator
- Reliefband Technologies (10022594)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- October 5, 2007
- Registered through
- 2026
- Brand names listed
- Reletex, Reliefband 1.5, Reliefband 50 Hours, Reliefband Classic, Reliefband Flex, Reliefband Premier, Reliefband Premier Plus, Reliefband Premier RB 2 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Complaint file establishment, Specification developer | 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 30, 2019 | K191547 | ReliefBand | GZJ | Substantially Equivalent | Reliefband Technologies, LLC | accessdata.fda.gov |
| June 21, 2019 | K182960 | ReliefBand | GZJ | Substantially Equivalent | Reliefband Technologies, LLC | accessdata.fda.gov |
| November 30, 2017 | K173233 | ReliefBand 1.5 | GZJ | Substantially Equivalent | Reliefband Technologies | accessdata.fda.gov |
| March 16, 2000 | K994387 | RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL | GZJ | Substantially Equivalent | Woodside Biomedical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 30, 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.