ClearanceBrief
Company ยท US

Visioncare Devices, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 2022. 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
HQEInstrument, Vitreous Aspiration And Cutting, Ac-Powered5
HQCUnit, Phacofragmentation1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 10, 2022K212763UniVit HE, UniVit UHS
Visioncare Devices, LLC
HQE
May 30, 2012K120170PROCARE PLUS VITRECTOMY SYSTEM
Visioncare Devices, Inc.
HQE
Apr 17, 2003K023939VELOCITY ADVANTAGE
Visioncare Devices, Inc.
HQE
Jun 9, 1997K971064BAYERS BIMANUAL I/A HANDPIECES
Visioncare Devices, Inc.
HQC
Jun 6, 1994K940746VIT CUTTER MODEL 94
Visioncare Devices, Inc.
HQE
Jan 28, 1991K904909I/A VITROPHAGE MODEL YPR 2001
Visioncare Devices, Inc.
HQE

Latest recalls

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