Data / Medical devices / United States / Paradigm Medical Technologies Corporation
Paradigm Medical Technologies Corporation: FDA-registered device maker in San Diego, CA, United States, 1 510(k) clearance
Paradigm Medical Technologies Corporation is registered with the FDA (registration 3025181200) in San Diego, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 3, 2022. Registered through 2027. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3025181200
- Address
- 7371 Los Brazos, San Diego, CA, United States, 92127
- Owner or operator
- Paradigm Medical Technologies Corporation (10091088)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- April 1, 2025
- Registered through
- 2027
- Brand names listed
- Multifrax
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument With MicrobeamFractional Output | ONG | 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 3, 2022 | K213332 | Multifrax Laser System | ONG | Substantially Equivalent | Paradigm Medical Corporation | accessdata.fda.gov |
Compare with other makers
Updated June 3, 2022. 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.