Data / Medical devices / United States / Zmicro, Inc.
Zmicro, Inc.: FDA-registered device maker in San Diego, CA, United States, 1 510(k) clearance
Zmicro, Inc. is registered with the FDA (registration 3008142630) in San Diego, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 12, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008142630
- Address
- 9820 Summers Ridge RD, San Diego, CA, United States, 92121
- Owner or operator
- Z Microsystems, Inc. (10046582)
- Roles
- Manufacturer
- First device listed
- April 9, 2014
- Registered through
- 2026
- Brand names listed
- Meridiem Surgical Video System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 12, 2013 | K130929 | ZMED VP4000 | LLZ | Substantially Equivalent | Zmed, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 12, 2013. 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.