FDA Device Intelligence
HomeDevice types › KKO

Ring, Teething, Fluid-Filled

FDA product code KKO · Class 2 · Dental

92
Registered devices
14
Adverse events
9
Recalls
27
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-12-02Tomy International Inc.Affected lots of the product are being recalled due to potential microbial growth in the fluid inside the device. if a compromised product is used by a child wi
2009-07-17Luv N' Care LtdGel filled teethers were found to contain to contain Bacillus circulans and Bacillus subtilis.
2009-07-07IMTEC CorporationSize printed on product packaging does not match size of enclosed product.
2006-01-25RC2 Brands Inc., The First YearsLiquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida
2006-01-25RC2 Brands Inc., The First YearsLiquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida
2006-01-25RC2 Brands Inc., The First YearsLiquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida
2006-01-25RC2 Brands Inc., The First YearsLiquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida
2006-01-25RC2 Brands Inc., The First YearsLiquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida
2006-01-25RC2 Brands Inc., The First YearsLiquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.