ClearanceBrief
Company ยท CN

Terumo Medical Products (Hangzhou) Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2025. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (2 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FPASet, Administration, Intravascular2
FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1
MOFGuide, Wire, Catheter, Neurovasculature1
PNDMidline Catheter1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 18, 2025K252402Midline Catheter
Terumo Medical Products (Hangzhou) Co., Ltd., CN
PND
Dec 17, 2025K252398SURFLO Hybria Closed System Safety IV Catheter
Terumo Medical Products (Hangzhou) Co., Ltd., CN
FOZ
Jun 23, 2023K221411Surflo Winged Infusion Set
Terumo Medical Products (Hangzhou) Co., Ltd., CN
FPA
Jun 29, 2022K220934RADIFOCUS Torque Device
Terumo Medical Products (Hangzhou) Co., Ltd., CN
MOF
May 30, 2003K031279SURSHIELD SAFETY WINGED BLOOD COLLECTION SET
Terumo Medical Products Hangzhou Co., Ltd.
FPA

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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