Data / Medical devices / United States / Aspen Livewell, LLC
Aspen Livewell, LLC: FDA-registered device maker in Lindon, UT, United States, 1 510(k) clearance
Aspen Livewell, LLC is registered with the FDA (registration 3011387816) in Lindon, UT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 30, 2014. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3011387816
- Address
- 175 N 1800 W Ste 108, Lindon, UT, United States, 84042
- Owner or operator
- Aspen LiveWell, LLC (10048301)
- Roles
- Complaint file establishment
- First device listed
- December 26, 2014
- Registered through
- 2027
- Brand names listed
- ALPINE Medical Therapy Laser Series, APEX - 6 Wavelength, 58 Watt Medical Laser System, APEX Medical Therapy Laser Series, ASCENT Medical Therapy Laser Series, PINNACLE Medical Therapy Laser Series, SUMMIT Medical Therapy Laser Series
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| October 30, 2014 | K142078 | VELASII THERAPY LASER SYSTEM | ILY | Substantially Equivalent | Aspen Laser Systems, LLC | accessdata.fda.gov |
Compare with other makers
Updated October 30, 2014. 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.