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Zhejiang Geyi Medical Instrument Co., Ltd.

FDA Regulatory Profile

Zhejiang Geyi Medical Instrument Co., Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 8, 2026.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Known Names

Zhejiang Geyi Medical Instrument Co, Zhejiang Geyi Medical Instrument

Recent 510(k) Clearances

K-NumberDeviceDate
K254294Single-use Digital Hysteroscope (GYUT-A 12.6- 0, GYUT-A12.6- 12, GYUT-A 12.6- 22, GYUT-A 12.6- 30, Sep 8, 2026
K252468Single-use Digital Flexible Ureteroscope (GY-UR9.3); Single-use Digital Flexible Ureteroscope (GY-URDec 16, 2025

FDA data resources