Data / Medical devices / United States / Transtimulation Research Inc
Transtimulation Research Inc: FDA-registered device maker in Pasadena, CA, United States, 2 510(k) clearances
Transtimulation Research Inc is registered with the FDA (registration 3036040187) in Pasadena, CA, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 9, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3036040187
- Address
- 898 N Fair Oaks Ave, Unit C, Pasadena, CA, United States, 91103
- Owner or operator
- Transtimulation Research, Inc (10092672)
- Roles
- Manufacturer
- First device listed
- February 4, 2025
- Registered through
- 2027
- Brand names listed
- Patch-TEA, TEA
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs) | QHH | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| April 9, 2025 | K243613 | Patch-TEA (Model TRI-21) | NUH | Substantially Equivalent | Transtimulation Research, Inc. | accessdata.fda.gov |
| September 14, 2023 | K230526 | TEA Device | QHH | Substantially Equivalent | Transtimulation Research, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs)
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated April 9, 2025. 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.