Spident Co., Ltd.
FDA 510(k) & PMA Approved Devices — 19 products
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Total Devices19
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K262983 | EsTemp Implant | EMA | 2026-09-25 | View |
| 510(k) | K262982 | Core·it Dual | EBF | 2026-09-21 | View |
| 510(k) | K262050 | Vioseal X | KIF | 2026-09-11 | View |
| 510(k) | K261129 | OrthoFit | DYH | 2026-07-02 | View |
| 510(k) | K250566 | EsCem RMGI | EMA | 2025-06-20 | View |
| 510(k) | K250317 | EsFlow PLUS | EBF | 2025-05-30 | View |
| 510(k) | K242702 | VioSeal | KIF | 2024-11-07 | View |
| 510(k) | K242675 | FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37 5ml, FineEtch 37% 1.2ml 20ea pack) | KLE | 2024-11-01 | View |
| 510(k) | K241445 | K-Bond Universal | KLE | 2024-07-22 | View |
| 510(k) | K231523 | EsCom250 | EBF | 2023-07-24 | View |
| 510(k) | K214076 | EsCem | EMA | 2022-12-19 | View |
| 510(k) | K214071 | Hexa-Temp | EBG | 2022-03-10 | View |
| 510(k) | K161774 | i-Sil | ELW | 2016-09-30 | View |
| 510(k) | K120767 | ES BOND | KLE | 2012-05-24 | View |
| 510(k) | K120768 | ES FLOW | EBF | 2012-05-03 | View |
| 510(k) | K110428 | ESCOM 100 | EBF | 2011-02-25 | View |
| 510(k) | K100413 | TEMP IT | EBF | 2010-03-03 | View |
| 510(k) | K100290 | ESTEMP NE | EMA | 2010-02-17 | View |
| 510(k) | K092572 | CORE*IT DUAL | EBF | 2009-08-26 | View |
No matching devices.
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