Dental Device Guide
Add your company

Not currently registered with FDA under this name

Sabre-K , Ltd.

Cheshire Wa 15 8ah, United Kingdom. Named as applicant on 1 dental 510(k) clearance between 1998 and 1998. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11998–1998
Markets registered in
1United States
Establishments
0—
1998: 11990200020102020

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Sabre-K , Ltd. as the applicant.

Decided510(k)DeviceDevice type
30 Sep 1998K983161KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOCELR Root Canal Post

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.