Not currently registered with FDA under this name

Osteoready, LLC

Concord, MA, United States. Named as applicant on 2 dental 510(k) clearances between 2015 and 2018. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 22015–2018
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Osteoready, LLC as the applicant.

Decided	510(k)	Device	Device type
17 Aug 2018	K173575	OsteoReady Dental Implant System	DZE Root-Form Endosseous Implant
8 Oct 2015	K151169	OsteoReady ZircoSeal Abutments	NHA Endosseous Dental Implant Abutment

Sources

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 of the most recent filing, which can be a US agent.