Data / Medical devices / United States / Reddrop DX
Reddrop DX: FDA-registered device maker in Fort Collins, CO, United States, 1 510(k) clearance
Reddrop DX is registered with the FDA (registration 3030747802) in Fort Collins, CO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 21, 2024. 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
- 3030747802
- Address
- 2401 Research Blvd #206, Fort Collins, CO, United States, 80526
- Owner or operator
- RedDrop Dx (10090542)
- Roles
- Specification developer
- First device listed
- April 10, 2024
- Registered through
- 2026
- Brand names listed
- RedDrop ONE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 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 |
|---|---|---|---|---|---|---|
| March 21, 2024 | K234081 | RedDrop ONE (One) | FMK | Unknown | Reddrop DX | accessdata.fda.gov |
Compare with other makers
Updated March 21, 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.