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Shandong Lianfa Medical Plastic Products Co. , Ltd.

FDA Regulatory Profile

Shandong Lianfa Medical Plastic Products 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 November 30, 2022.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K222472Lancing System, Sterile Lancet for Single Use, Lancing DeviceNovember 30, 2022
K222376Lianfa Safety Lancet (Five Models: NPA, PA, PA2, TPA, and APA)October 3, 2022

FDA data resources