Data / Medical devices / United States / Chirp Innovation, LLC
Chirp Innovation, LLC: FDA-registered device maker in Lehi, UT, United States, 1 510(k) clearance
Chirp Innovation, LLC is registered with the FDA (registration 3020769982) in Lehi, UT, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 27, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3020769982
- Address
- 3900 N Traverse Mountain Blvd Suite 300, Lehi, UT, United States, 84043
- Owner or operator
- Chirp Innovation, LLC (10083092)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- July 3, 2024
- Registered through
- 2026
- Brand names listed
- Chirp Contour, Chirp Halo, Chirp RPM, Chirp Wheel, TENS&EMS units (SM9109A, SM9109B)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Electric | ISA | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 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 |
|---|---|---|---|---|---|---|
| June 27, 2024 | K241509 | TENS&EMS units (SM9109A, SM9109B) | NUH | Substantially Equivalent | Plexus Yoga, LLC Dba Chirp | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Manual
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Massager, Therapeutic, Electric
Updated June 27, 2024. 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.