Data / Medical devices / United States / Verdure Imaging Inc
Verdure Imaging Inc: FDA-registered device maker in Stockton, CA, United States, 1 510(k) clearance
Verdure Imaging Inc is registered with the FDA (registration 3035373446) in Stockton, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 7, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035373446
- Address
- 4560 N Pershing Ave Ste B, Stockton, CA, United States, 95207
- Owner or operator
- Verdure Imaging Inc (10090521)
- Roles
- Manufacturer
- First device listed
- January 6, 2025
- Registered through
- 2026
- Brand names listed
- SpineUs
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automated Radiological Image Processing Software | QIH | 2 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Manufacturer | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 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 |
|---|---|---|---|---|---|---|
| October 7, 2024 | K241029 | SpineUs System | IYO | Substantially Equivalent | Verdure Imaging | accessdata.fda.gov |
Compare with other makers
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
- All makers of Automated Radiological Image Processing Software
- All makers of Transducer, Ultrasonic, Diagnostic
Updated October 7, 2024. 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.