Data / Medical devices / United States / Synaptic Tech, LLC
Synaptic Tech, LLC: FDA-registered device maker in Los Angeles, CA, United States, 1 510(k) clearance
Synaptic Tech, LLC is registered with the FDA (registration 3016660162) in Los Angeles, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 4, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016660162
- Address
- 11500 West Olympic BLVD Suite 400, Los Angeles, CA, United States, 90064
- Owner or operator
- Synaptic Tech, LLC (10064191)
- Roles
- Manufacturer
- First device listed
- March 24, 2020
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Biofeedback | HCC | 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 |
|---|---|---|---|---|---|---|
| August 4, 1995 | K945826 | J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS | HCC | Substantially Equivalent | Medical Device Inspection Co., Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 4, 1995. 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.