FDA 510(k) Applications Submitted by MegaGen Implant CO., Ltd.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K123870 |
12/17/2012 |
XPEED ANYRIDGE INTERNAL IMPLANT SYSTEM |
MEGAGEN IMPLANT CO., LTD. |
K223339 |
11/01/2022 |
Bone Chamber Implant |
MegaGen Implant Co., Ltd. |
K190096 |
01/22/2019 |
R2GATE |
MegaGen Implant Co., Ltd. |
K182448 |
09/07/2018 |
AnyRidge Octa 1 Implant System |
MegaGen Implant Co., Ltd. |
K211812 |
06/11/2021 |
BLUEDIAMOND IMPLANT, Abutment Screw |
MegaGen Implant Co., Ltd. |
K220562 |
02/28/2022 |
TiGEN Abutment, ZrGEN Abutment and Scan Healing Abutment |
MegaGen Implant Co., Ltd. |
K211556 |
05/19/2021 |
N2 |
MegaGen Implant Co., Ltd. |
K191127 |
04/29/2019 |
Advanced Intermezzo Implant System |
MegaGen Implant Co., Ltd. |
K222219 |
07/25/2022 |
R2 Studio Q/RCT820 |
MegaGen Implant CO., Ltd. |
K203554 |
12/04/2020 |
AnyOne External Implant System |
MegaGen Implant Co., Ltd. |
K210161 |
01/21/2021 |
AnyOne Onestage Implant System |
MegaGen Implant Co., Ltd. |
K210826 |
03/19/2021 |
Healing Abutment, Cover Screw |
MegaGen Implant Co., Ltd. |
K192614 |
09/23/2019 |
Meg-Ball Attachment System, Meg-Loc Abutment, Meg-Magnet Abutment |
MegaGen Implant CO., Ltd. |
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