Data / Medical devices / United States / Natera Inc.
Natera Inc.: FDA-registered device maker in San Carlos, CA, United States, 1 PMA approval
Natera Inc. is registered with the FDA (registration 3010889807) in San Carlos, CA, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated May 15, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010889807
- Address
- 201 Industrial Rd Ste 410, San Carlos, CA, United States, 94070
- Owner or operator
- Natera INC. (10095611)
- Roles
- Manufacturer
- First device listed
- May 27, 2026
- Registered through
- 2026
- Brand names listed
- Natera, Inc.
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System | PQP | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| May 15, 2026 | P260004 | Signatera CDx | PQP | 0 | May 15, 2026 | accessdata.fda.gov |
Compare with other makers
Updated May 15, 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.