Data / Medical devices / United States / Onocor LLC
Onocor LLC: FDA-registered device maker in West Chester, PA, United States, 1 510(k) clearance
Onocor LLC is registered with the FDA (registration 3023548693) in West Chester, PA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 23, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023548693
- Address
- 1570 Pocopson Rd, West Chester, PA, United States, 19382
- Owner or operator
- Onocor LLC (10085947)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- September 16, 2022
- Registered through
- 2026
- Brand names listed
- ONO
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Percutaneous Retrieval | MMX | 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 |
|---|---|---|---|---|---|---|
| May 23, 2022 | K212988 | ONO Retrieval Device | MMX | Substantially Equivalent | Onocor Vascular, LLC | accessdata.fda.gov |
Compare with other makers
Updated May 23, 2022. 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.