ClearanceBrief
Company ยท US

Technolas Perfect Vision GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2020. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OOEOphthalmic Femtosecond Laser9
MXKDevice, Analysis, Anterior Segment1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 1, 2020K200724VICTUS Femtosecond Laser Platform
Technolas Perfect Vision GmbH, DE
OOE
Oct 19, 2017K171014VICTUS Femtosecond Laser Platform
Technolas Perfect Vision GmbH, DE
OOE
Jun 24, 2015K151161VICTUS Femtosecond Laser Platform
Technolas Perfect Vision GmbH, DE
OOE
Jan 16, 2015K141379VICTUS FEMTOSECOND LASER PLATFORM
Technolas Perfect Vision GmbH
OOE
Jul 15, 2014K140615VICTUS FEMTOSECOND LASER PLATFORM
Technolas Perfect Vision GmbH
OOE
Feb 14, 2014K132534VICTUS FEMTOSECOND LASER PLATFORM
Technolas Perfect Vision GmbH
OOE
Feb 8, 2013K122386VICTUS FEMTOSECOND LASER PLATFORM
Technolas Perfect Vision GmbH
OOE
Jul 31, 2012K120426VICTUS LASER PLATFORM
Technolas Perfect Vision GmbH
OOE
Nov 22, 2011K110427FEMTEC LASER SYSTEM FOR CAPSULOTOMY
Technolas Perfect Vision GmbH
OOE
Mar 5, 1999K984443ORBSCAN
Technolas Perfect Vision GmbH
MXK

Latest recalls

DateFirm and productCodeLinked 510(k)
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