Manufacturer registered with FDA

Kids II

Atlanta, GA, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.

FDA owner/operator10027029Specification developer

Device types listed: 2
Brands and models: 0
510(k) clearances: 22009–2011
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2000–2026

Devices listed with FDA

What Kids II currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Fluid-Filled Teething RingKKO · Class 2	—	Maker	—	2011
Teething Ring Non-Fluid FilledMEF · Class 1	—	Maker	—	2009

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Kids II as the applicant.

Decided	510(k)	Device	Device type
27 Jan 2011	K092025	FLUID FILLED TEETHER - GEL	KKO Fluid-Filled Teething Ring
27 May 2009	K082824	FLUID FILLED TEETHER	KKO Fluid-Filled Teething Ring

Registered establishments

Establishment	Location	What it does
KIDS II, INC.FDA reg. 3007154355	Atlanta, GA, United States	Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10027029). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.