Medical Device Manufacturer · KR , Incheon

Spident Co., Ltd. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2009

Recent clearances: EsTemp Implant, Core·it Dual, Vioseal X

Total

Cleared

Denied

Spident Co., Ltd. has 21 FDA 510(k) cleared dental devices. Based in Incheon, KR.

Latest FDA clearance: Sep 2026. Active since 2009.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Spident USA, Inc..

Spident Co., Ltd. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Spident Co., Ltd.

21 devices

1-12 of 21

FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37...

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Oct 05, 2026

Spident Co., Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Spident Co., Ltd.

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