Data / Medical devices / United States / Exact Sciences Corporation- Legacy Campus
Exact Sciences Corporation- Legacy Campus: FDA-registered device maker in Madison, WI, United States, 1 PMA approval
Exact Sciences Corporation- Legacy Campus is registered with the FDA (registration 3013841562) in Madison, WI, United States. It lists 4 device types. The FDA files 1 PMA approval under its listings, the newest dated August 11, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013841562
- Address
- 320 Holtzman Road, Madison, WI, United States, 53713
- Owner or operator
- Exact Sciences Corporation (10047364)
- Roles
- Manufacturer
- First device listed
- August 18, 2014
- Registered through
- 2026
- Brand names listed
- Capture Aspirator, Capture Incubator, Capture Incubator 2, Cologuard, 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 |
| Station, Pipetting And Diluting, For Clinical Use | JQW | 1 | Manufacturer | accessdata.fda.gov |
| System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection | PHP | 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 |
|---|---|---|---|---|---|---|
| August 11, 2014 | P130017 | COLOGUARD | PHP | 69 | June 9, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of Bath, Incubators/Water, All
- All makers of Blender/Mixer
- All makers of System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection
- All makers of Station, Pipetting And Diluting, For Clinical Use
Updated June 9, 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.