Shanghai Sanyou Medical Co, Ltd.

FDA Regulatory Profile

Shanghai Sanyou Medical Co, Ltd. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 12, 2023.

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Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K230872Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction Changeable Lumbar…Dec 12, 2023
K230961Zeus Spinal SystemOct 10, 2023
K231931Adena-Zina Spinal SystemJul 28, 2023
K211689KEYSTONE PEEK Cage SystemSep 21, 2021
K212066Adena-Zina SystemAug 16, 2021
K163366Shanghai Sanyou CARMEN Cervical Fusion SystemOct 5, 2017
K163422Shanghai Sanyou PEEK Cage SystemSep 18, 2017
K152781Adena-Zina SystemFeb 12, 2016
K131512KATIA SYSTEMAug 7, 2013