Data / Medical devices / United States / Carbon, Inc.
Carbon, Inc.: FDA-registered device maker in Sunnyvale, CA, United States, 1 510(k) clearance
Carbon, Inc. is registered with the FDA (registration 3046274075) in Sunnyvale, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 2, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3046274075
- Address
- 1272 Borregas Ave, Sunnyvale, CA, United States, 94089
- Owner or operator
- Carbon, Inc. (10096249)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- August 6, 2026
- Registered through
- 2026
- Brand names listed
- DB4000 High Impact Denture Base
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 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 2, 2026 | K260569 | DB 4000 High Impact Denture Base | EBI | Substantially Equivalent | Carbon, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 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.