ClearanceBrief
Company ยท US

Alcon Manufacturing, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2012. Name variants (Inc, Corp, punctuation) are merged.

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

Product codes

CodeDeviceRecords
HQCUnit, Phacofragmentation4
KYBLens, Guide, Intraocular1
MSSFolders And Injectors, Intraocular Lens (Iol)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 15, 2012K120912INFINITI(R) VISION SYSTEM
Alcon Manufacturing, Ltd.
HQC
Nov 21, 2011K112425INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE
Alcon Manufacturing, Ltd.
HQC
Oct 13, 2011K101774MONARCH III IOL DELIVERY SYSTEM; MONARCH III P CATRIDGE; MONARCH III HANDPIECE (H4)
Alcon Manufacturing, Ltd.
MSS
Nov 12, 2010K101285CONSTELLATION VISION SYSTEM
Alcon Manufacturing, Ltd.
HQC
Mar 4, 2010K093210AQUALASE CAPSULE WASH TIP
Alcon Manufacturing, Ltd.
HQC
Mar 27, 2007K063155MONARCH III IOL DELIVERY SYSTEM
Alcon Manufacturing, Ltd.
KYB

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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