Spident Co., Ltd.
Spident Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2026.
Top product codes for Spident Co., Ltd.
Recent clearances by Spident Co., Ltd.
- K262050 — Vioseal X
- K261129 — OrthoFit
- K250566 — EsCem RMGI
- K250317 — EsFlow PLUS
- K242702 — VioSeal
- K242675 — FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37 5ml, FineEtch 37% 1.2ml 20ea pack)
- K241445 — K-Bond Universal
- K231523 — EsCom250
- K214076 — EsCem
- K214071 — Hexa-Temp
- K161774 — i-Sil
- K134022 — BASE IT
- K134021 — ESTEMP IMPLANT, ESTEMP CLEAR
- K120767 — ES BOND
- K120768 — ES FLOW
- K110428 — ESCOM 100
- K100413 — TEMP IT
- K100290 — ESTEMP NE
- K092572 — CORE*IT DUAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.