Data / Medical devices / Ring, Teething, Non-Fluid Filled / United States
FDA-registered makers of Ring, Teething, Non-Fluid Filled in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Ring, Teething, Non-Fluid Filled (product code MEF). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Ring, Teething, Non-Fluid Filled
- Product code
- MEF
- Country
- United States
Makers of Ring, Teething, Non-Fluid Filled in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Casco Bay Molding | Sanford, ME, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dr. Brown's Company | Saint Louis, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kids Ii, Inc. | Atlanta, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Luv N' Care, Ltd. | Monroe, LA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nuk Usa LLC | Reedsburg, WI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ouachita Contract Manufacturing, LLC | Monroe, LA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oogie Solutions LLC | Potomac, MD, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quintessential Tots, LLC | Naperville, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sassy Baby, Inc | Gonzales, LA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Small Beginnings Inc. | Hesperia, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Talbot's Pharmaceuticals Family Products LLC | Monroe, LA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.