Data / Medical devices / United States / U Deliver Medical L.L.C.
U Deliver Medical L.L.C.: FDA-registered device maker in Hopkins, MN, United States, 2 510(k) clearances
U Deliver Medical L.L.C. is registered with the FDA (registration 3014016859) in Hopkins, MN, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 31, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014016859
- Address
- 7900 Excelsior BLVD Ste 108, Hopkins, MN, United States, 55343
- Owner or operator
- U Deliver Medical, LLC (10055940)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- October 25, 2017
- Registered through
- 2026
- Brand names listed
- Bolink, Bolink(TM) Larger Cap Gravity Set, Bolink(TM) Small Cap Gravity Set
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Gastrointestinal Tubes With Enteral Specific Connectors | PIF | 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 31, 2019 | K190310 | U Deliver Bolink ENFit Enteral Feeding Sets | PIF | Substantially Equivalent | U Deliver Medical, LLC | accessdata.fda.gov |
| August 17, 2017 | K170555 | U Deliver Bolink ENFit Enteral Feeding Sets | PIF | Substantially Equivalent | U Deliver Medical, LLC | accessdata.fda.gov |
Compare with other makers
Updated May 31, 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.