FDA 510(k) Applications Submitted by Spident Co., Ltd.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K231523 |
05/26/2023 |
EsCom250 |
Spident Co., Ltd. |
| K100290 |
02/02/2010 |
ESTEMP NE |
SPIDENT CO., LTD. |
| K100413 |
02/16/2010 |
TEMP IT |
SPIDENT CO., LTD. |
| K120767 |
03/14/2012 |
ES BOND |
SPIDENT CO., LTD. |
| K120768 |
03/14/2012 |
ES FLOW |
SPIDENT CO., LTD. |
| K092572 |
08/21/2009 |
CORE*IT DUAL |
SPIDENT CO., LTD. |
| K161774 |
06/28/2016 |
i-Sil |
SPIDENT Co., Ltd. |
| K214071 |
12/27/2021 |
Hexa-Temp |
SPIDENT CO., LTD. |
| K214076 |
12/27/2021 |
EsCem |
SPIDENT CO., LTD. |
| K110428 |
02/14/2011 |
ESCOM 100 |
SPIDENT CO., LTD. |
| K134021 |
12/30/2013 |
ESTEMP IMPLANT, ESTEMP CLEAR |
SPIDENT CO., LTD. |
| K134022 |
12/30/2013 |
BASE IT |
SPIDENT CO., LTD. |
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