Data / Medical devices / United States / Ideate Medical
Ideate Medical: FDA-registered device maker in Saint Louis, MO, United States, 1 510(k) clearance
Ideate Medical is registered with the FDA (registration 3043237009) in Saint Louis, MO, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 27, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043237009
- Address
- 2821 N Ballas Rd Ste C55, Saint Louis, MO, United States, 63131
- Owner or operator
- IDEATE MEDICAL (10095230)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- February 9, 2026
- Registered through
- 2026
- Brand names listed
- Biopsy Connector Type 1, Biopsy Connector Type 2, Insert Connector Assembly Large Type 2, Insert Connector Assembly Small Type 1, Insert Connector Medium Type 1, Luer Connector Type 1, Pipette Connector Type 1, Pipette Connector Type 2 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | KCT | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Sterilizer, Chemical | MLR | 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 27, 2024 | K233762 | SteroScope® Sterilization Technology System | MLR | Substantially Equivalent | Ideate Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Sterilizer, Chemical
- All makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Updated June 27, 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.