Data / Medical devices / United States / J3 Bioscience, Inc.
J3 Bioscience, Inc.: FDA-registered device maker in Salt Lake City, UT, United States, 1 510(k) clearance
J3 Bioscience, Inc. is registered with the FDA (registration 3021574111) in Salt Lake City, UT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 20, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021574111
- Address
- 825 North 300 West, Suite N231, Salt Lake City, UT, United States, 84103
- Owner or operator
- J3 Bioscience, Inc. (10083638)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- December 22, 2021
- Registered through
- 2026
- Brand names listed
- LivRing
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Personal Lubricant Ring | QPD | 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 20, 2021 | K203377 | VR101 Lubricating Intravaginal Ring | QPD | Substantially Equivalent | J3 Bioscience, Inc. | accessdata.fda.gov |
Updated May 20, 2021. 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.