Data / Medical devices / United States / Seven Hills Pharmacy LLC
Seven Hills Pharmacy LLC: FDA-registered device maker in Sharonville, OH, United States, 1 510(k) clearance
Seven Hills Pharmacy LLC is registered with the FDA (registration 3026032436) in Sharonville, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 7, 2019. 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
- 3026032436
- Address
- 2722 E. Kemper Rd, Sharonville, OH, United States, 45241
- Owner or operator
- Seven Hills Pharmacy LLC (10086907)
- Roles
- Repackager or relabeler
- First device listed
- January 17, 2023
- Registered through
- 2026
- Brand names listed
- Seven Hills Pharmacy
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Integrated Continuous Glucose Monitoring System For Professional Directed Retrospective Or Real-Time Use | QII | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| October 7, 2019 | K191833 | Dexcom G6 Pro Continuous Glucose Monitoring System | QII | Substantially Equivalent | Dexcom, Inc. | accessdata.fda.gov |
Updated October 7, 2019. 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.