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Rxsight, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231838RxSight® Insertion Device (63002)August 15, 2023
K231466RxSight Insertion DeviceJune 12, 2023
K201909RxSight Contact LensSeptember 10, 2020
K192926RxSight Insertion DeviceJanuary 17, 2020
K181401RxSight Insertion DeviceJuly 26, 2018