Data / Medical devices / United States / Exact Sciences Corporation- Discovery Campus
Exact Sciences Corporation- Discovery Campus: FDA-registered device maker in Madison, WI, United States, 3 PMA approvals
Exact Sciences Corporation- Discovery Campus is registered with the FDA (registration 3015728010) in Madison, WI, United States. It lists 5 device types. The FDA files 3 PMA approvals under its listings, the newest dated July 24, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3015728010
- Address
- 650 Forward Dr, Madison, WI, United States, 53711
- Owner or operator
- Exact Sciences Corporation (10047364)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- August 18, 2014
- Registered through
- 2026
- Brand names listed
- Capture Aspirator, Capture Incubator, Capture Incubator 2, Cologuard, Cologuard Plus, Conversion Wash 2 (Concentrate), Sample Mixer, Sample Mixer 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bath, Incubators/Water, All | JTQ | 1 | Manufacturer | accessdata.fda.gov |
| Blender/Mixer | JRO | 1 | Manufacturer | accessdata.fda.gov |
| General Purpose Reagent | PPM | 1 | Manufacturer | accessdata.fda.gov |
| Station, Pipetting And Diluting, For Clinical Use | JQW | 1 | Manufacturer | accessdata.fda.gov |
| System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection | PHP | 3 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| July 24, 2026 | P250029 | SimpleScreen CRC | PHP | 1 | August 26, 2026 | accessdata.fda.gov |
| October 3, 2024 | P230043 | Multi-Target Stool DNA (mtsDNA) Test, Cologuard Plus | PHP | 10 | August 3, 2026 | accessdata.fda.gov |
| August 11, 2014 | P130017 | COLOGUARD | PHP | 69 | June 9, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of Station, Pipetting And Diluting, For Clinical Use
- All makers of Blender/Mixer
- All makers of System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
- All makers of Bath, Incubators/Water, All
- All makers of General Purpose Reagent
Updated August 26, 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.