Data / Medical devices / United States / Claria Medical
Claria Medical: FDA-registered device maker in Mountain View, CA, United States, 1 510(k) clearance
Claria Medical is registered with the FDA (registration 3023620966) in Mountain View, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 2, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023620966
- Address
- 2586 Wyandotte St, Mountain View, CA, United States, 94043
- Owner or operator
- Claria Medical (10091256)
- Roles
- Complaint file establishment, Manufacturer, Manufacturer for export
- First device listed
- August 2, 2024
- Registered through
- 2026
- Brand names listed
- Claria BTR, Claria Bulk Tissue Reducer, Claria Console, Claria Container, Claria Handpiece, Claria System, Claria Tenaculum
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Clamp, Uterine | HGC | 1 | Complaint file establishment, Manufacturer, Manufacturer for export | accessdata.fda.gov |
| Containment System, Laparoscopic Power Morcellation, With Instrument Port | PMU | 2 | Manufacturer for export | accessdata.fda.gov |
| Gynecologic Power Morcellator And Containment System | SIM | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| July 2, 2026 | DEN250034 | Claria System | SIM | Unknown | Claria Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Containment System, Laparoscopic Power Morcellation, With Instrument Port
- All makers of Gynecologic Power Morcellator And Containment System
- All makers of Clamp, Uterine
Updated July 2, 2026. 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.