ClearanceBrief
Company ยท US

The Lagado Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2013. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HQDLens, Contact (Other Material) - Daily3
LPLLenses, Soft Contact, Daily Wear1
LRXCase, Contact Lens1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 13, 2013K120756LSH (MANGOFILCON A) SPHERE SOFT (HYDROPHILIC) CONTACT LENS, LSH (MANGOFILCON A) MULTIFOCAL SOFT (HYDROPHILIC) CONTACT LE
The Lagado Corp.
LPL
Apr 3, 2013K130285PROGENT LARGE DIAMETER CONTACT LENS CASE FOR RIGID GAS PERMEABLE LENS
The Lagado Corp.
LRX
Jan 21, 2011K102154TYRO-97 (HOFOCON A), ONSI 56 (HOFOCON), RIGID GAS PERMEABLE SPHERICAL, ASPHERIC, TORIC AND BIFOCAL CONTACT LENS
The Lagado Corp.
HQD
Nov 2, 2005K052507TYRO 97 (HOFOCON A) RIGID GAS PERMEABLE SPHERICAL, ASPHERIC, TORIC AND BIFOCAL CONTACT LENSES FOR DAILY WEAR
The Lagado Corp.
HQD
Sep 16, 2004K033599ONSI -56 (ONSIFOCON A) RIGID GAS PERMEABLE SPHERICAL, ASPHERIC, TORIC AND BIFOCAL CONTACT LENS
The Lagado Corp.
HQD

Latest recalls

DateFirm and productCodeLinked 510(k)
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