Data / Medical devices / United States / Telli Health LLC
Telli Health LLC: FDA-registered device maker in Mcallen, TX, United States, 1 510(k) clearance
Telli Health LLC is registered with the FDA (registration 3017075369) in Mcallen, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 21, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017075369
- Address
- 801 E Fir Ave, Mcallen, TX, United States, 78501
- Owner or operator
- Telli Health LLC (10075949)
- Roles
- Complaint file establishment
- First device listed
- April 22, 2026
- Registered through
- 2026
- Brand names listed
- Telli Health NIBP Model 2006-2B
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 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 |
|---|---|---|---|---|---|---|
| September 21, 2020 | K201467 | Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B | DXN | Substantially Equivalent | Bioland Technology, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 21, 2020. 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.