Data / Medical devices / United States / Kids Ii, Inc.
Kids Ii, Inc.: FDA-registered device maker in Atlanta, GA, United States, 1 510(k) clearance
Kids Ii, Inc. is registered with the FDA (registration 3007154355) in Atlanta, GA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 27, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007154355
- Address
- 3333 Piedmont Rd NE Suite 1800, Atlanta, GA, United States, 30305
- Owner or operator
- Kids II (10027029)
- Roles
- Specification developer
- First device listed
- June 2, 2009
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Ring, Teething, Fluid-Filled | KKO | 2 | Specification developer | accessdata.fda.gov |
| Ring, Teething, Non-Fluid Filled | MEF | 1 | 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 |
|---|---|---|---|---|---|---|
| January 27, 2011 | K092025 | FLUID FILLED TEETHER - GEL | KKO | Substantially Equivalent | Kids II | accessdata.fda.gov |
Compare with other makers
Updated January 27, 2011. 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.