Data / Medical devices / United States / Algiamed Technologies Usa Inc
Algiamed Technologies Usa Inc: FDA-registered device maker in Lake Mary, FL, United States, 1 510(k) clearance
Algiamed Technologies Usa Inc is registered with the FDA (registration 3037967280) in Lake Mary, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 18, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3037967280
- Address
- 801 International Pkwy Fl 5, Lake Mary, FL, United States, 32746
- Owner or operator
- Algiamed Technologies USA Inc (10091878)
- Roles
- Manufacturer
- First device listed
- April 8, 2025
- Registered through
- 2026
- Brand names listed
- STIMPOD NMS460 Nerve Stimulator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 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 |
|---|---|---|---|---|---|---|
| January 18, 2017 | K161091 | STIMPOD NMS460 Nerve Stimulator | GZJ | Substantially Equivalent | Xavant Technology (Pty), Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 18, 2017. 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.