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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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