Sabre-K , Ltd.

Sabre-K , Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 1998.

Top product codes for Sabre-K , Ltd.

ELR — Dental1 device

Recent clearances by Sabre-K , Ltd.

K983161 — KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOCCode ELR·1998-09-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.