Data / Medical devices / United States / Mobilehelp LLC
Mobilehelp LLC: FDA-registered device maker in Philadelphia, PA, United States, 1 510(k) clearance
Mobilehelp LLC is registered with the FDA (registration 3008101184) in Philadelphia, PA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 11, 2010. Registered through 2026. 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
- 3008101184
- Address
- 1818 Market St Suite 1200, Philadelphia, PA, United States, 19103
- Owner or operator
- MobileHelp LLC (10042590)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- June 16, 2015
- Registered through
- 2026
- Brand names listed
- Clear Arch Classic RPM, Clear Arch Mobile, Clear Arch Touch, Genesis DM, Genesis DM Pro BP, Genesis Touch, Genesis Touch Remote Patient Monitoring System, Genesis Touch System and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Medical Device Data System | OUG | 1 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Transmitters And Receivers, Physiological Signal, Radiofrequency | DRG | 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 |
|---|---|---|---|---|---|---|
| June 11, 2010 | K101242 | GENESIS DM MODEL: 6053000A1 | DRG | Substantially Equivalent | Honeywell Hommed, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Medical Device Data System
- All makers of Transmitters And Receivers, Physiological Signal, Radiofrequency
Updated June 11, 2010. 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.