Data / Medical devices / United States / Intuitap Medical, Inc
Intuitap Medical, Inc: FDA-registered device maker in Chicago, IL, United States, 1 510(k) clearance
Intuitap Medical, Inc is registered with the FDA (registration 3027594726) in Chicago, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 19, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3027594726
- Address
- 1623 W Fulton St (IntuiTap mHUB), Chicago, IL, United States, 60612
- Owner or operator
- IntuiTap Medical, Inc (10095409)
- Roles
- Specification developer
- First device listed
- March 10, 2026
- Registered through
- 2026
- Brand names listed
- VerTouch, VerTouch+
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Spinal Imaging System For Neuraxial Procedures | QXD | 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 |
|---|---|---|---|---|---|---|
| January 19, 2024 | DEN220009 | VerTouch Spinal Imaging Device | QXD | Unknown | Intuitap Medical, Inc. | accessdata.fda.gov |
Updated January 19, 2024. 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.