ClearanceBrief
Company · JP

Kitazato Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2026. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MQLMedia, Reproductive8
MQFCatheter, Assisted Reproduction3
MQENeedle, Assisted Reproduction1
MQKLabware, Assisted Reproduction1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 28, 2026K260248Ultra-Fast Warm
Kitazato Corporation, JP
MQL
Aug 26, 2025K251305Ultra-Fast Vitri; Ultra-Fast Warm
Kitazato Corporation, JP
MQL
Oct 23, 2020K200249Sequential Culture Media (Fertilization Medium [without HSA/rHA, with HSA, with rHA], Cleavage Medium [without HSA/rHA,
Kitazato Corporation, JP
MQL
Aug 25, 2020K193522iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHA
Kitazato Corporation, JP
MQL
Aug 17, 2020K192845Sperm Freeze, Sperm Fridge
Kitazato Corporation, JP
MQL
May 1, 2020K192540Kitazato ET Catheters
Kitazato Corporation, JP
MQF
Sep 26, 2019K190199SepaSperm Washing Solution, SepaSperm Solution
Kitazato Corporation, JP
MQL
Nov 9, 2018K181469Cryotop®US-flash and Cryotop®US-scoop
Kitazato Corporation, JP
MQK
Oct 23, 2018K182002Cumulus Remover
Kitazato Corporation, JP
MQL
Dec 14, 2017K171748Vitrification Kit and Thawing Kit
Kitazato Corporation, JP
MQL
Jul 13, 2017K162878Kitazato ET Catheters
Kitazato Corporation, JP
MQF
Jul 11, 2017K162881Kitazato OPU Needles
Kitazato Corporation, JP
MQE
May 11, 2017K162667Kitazato IUI Catheter
Kitazato Corporation, JP
MQF

Latest recalls

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