Data / Medical devices / United States / Nano4imaging Usa, LLC.
Nano4imaging Usa, LLC.: FDA-registered device maker in Dublin, OH, United States, 1 510(k) clearance
Nano4imaging Usa, LLC. is registered with the FDA (registration 3015522130) in Dublin, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 6, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015522130
- Address
- 7239 Sawmill Rd, Dublin, OH, United States, 43016
- Owner or operator
- Nano4imaging USA, LLC (10060787)
- Roles
- Complaint file establishment
- First device listed
- May 4, 2026
- Registered through
- 2026
- Brand names listed
- EmeryGlide
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wire, Guide, Catheter | DQX | 2 | Complaint file establishment | 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 6, 2026 | K253262 | EmeryGlide (EG18008901) | DQX | Substantially Equivalent | Nano4imaging GmbH | accessdata.fda.gov |
Compare with other makers
Updated March 6, 2026. 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.