FDA 510(k) Applications Submitted by Osstem Implant Co., Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K160519 02/25/2016 Link Abutment for CEREC Osstem Implant Co., Ltd
K153015 10/15/2015 Transfer & Angled Abutment Osstem Implant Co., Ltd
K151262 05/13/2015 Hyflex Heavy, Hyflex Mono, Hyflex Light Osstem Implant Co., Ltd
K123755 12/07/2012 MULTI ANGLED ABUTMENT OSSTEM IMPLANT CO., LTD


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