Data / Medical devices / United States / Uberlube
Uberlube: FDA-registered device maker in Skokie, IL, United States, 1 510(k) clearance
Uberlube is registered with the FDA (registration 3012482333) in Skokie, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 23, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012482333
- Address
- 7316 Ridgeway AVe., Skokie, IL, United States, 60076
- Owner or operator
- Uberlube Inc. (10051831)
- Roles
- Manufacturer
- First device listed
- May 9, 2016
- Registered through
- 2026
- Brand names listed
- Uberlube
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| September 23, 2015 | K151647 | Uberlube | NUC | Substantially Equivalent | Uberlube, LLC | accessdata.fda.gov |
Compare with other makers
Updated September 23, 2015. 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.