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Beijing Globalipl Development Co., Ltd.

FDA Regulatory Profile

Beijing Globalipl Development Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 9, 2022.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222916US 450 Diode Laser EquipmentDecember 9, 2022
K220385Intense Pulsed Light EquipmentAugust 12, 2022
K212611CO2 Laser EquipmentFebruary 1, 2022
K193328IPL + Diode Laser MachineMarch 25, 2020

FDA data resources