Data / Medical devices / United States / Interfocus Inc.
Interfocus Inc.: FDA-registered device maker in Mountain View, CA, United States, 1 510(k) clearance
Interfocus Inc. is registered with the FDA (registration 3043515178) in Mountain View, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043515178
- Address
- 650 Castro Street, Ste, Mountain View, CA, United States, 94041
- Owner or operator
- Interfocus Inc. (10095183)
- Roles
- Specification developer
- First device listed
- February 4, 2026
- Registered through
- 2026
- Brand names listed
- Electric Breast Pump(Model: H03)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Breast, Powered | HGX | 2 | 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 |
|---|---|---|---|---|---|---|
| December 19, 2025 | K252342 | Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810) | HGX | Substantially Equivalent | Guangdong Youmeng Electrical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 19, 2025. 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.