ClearanceBrief
Company · US

Rxsight, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MSSFolders And Injectors, Intraocular Lens (Iol)5
HJKLens, Contact, Polymethylmethacrylate, Diagnostic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 10, 2026K261174RxSight® Insertion Device
Rxsight, Inc.
MSS
Aug 15, 2023K231838RxSight® Insertion Device (63002)
Rxsight, Inc.
MSS
Jun 12, 2023K231466RxSight Insertion Device
Rxsight, Inc.
MSS
Sep 10, 2020K201909RxSight Contact Lens
Rxsight, Inc.
HJK
Jan 17, 2020K192926RxSight Insertion Device
Rxsight, Inc.
MSS
Jul 26, 2018K181401RxSight Insertion Device
Rxsight, Inc.
MSS

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes