510(k) Report

510(k) · Cleared

Cleared

VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient Medium

K212410510(k) TraditionalCleared Feb 1, 2022182-day reviewClass II21 CFR 884.6180

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Shenzhen Vitavitro Biotech Co., Ltd. · MQL Media, Reproductive

Cleared on Feb 1, 2022 as substantially equivalent to K190199 (Kitazato Corporation, 2019) after a 182-day review. Its family tree reaches back 3 generations to 2000. 1 later device descends from it.

Decided
Feb 1, 2022
Review
182 days
Class
Class II
Product code
MQL
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K002383 (2000). 1 later device descends from it, 1 citing it directly.

  1. Root · 3 generations backK002383 Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm…Cook Ob/Gyn · 2000
  2. 2 generations backK152782 Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf…William A. Cook Australia Pty., Ltd. · 2015
  3. 1 generation backK190199 SepaSperm Washing Solution, SepaSperm SolutionKitazato Corporation · 2019
  4. This deviceK212410 VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient MediumShenzhen Vitavitro Biotech Co., Ltd. · 2022
  5. Descendant · cites it directly · 0 of its ownK241095 ARTSMedia Semen Wash MediumArtsmedia Denmark Aps · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K241095ARTSMedia Semen Wash MediumArtsmedia Denmark Aps · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K002383Cook Ivf Sperm Buffer, Cook Ivf Sperm Medium, and Cook Ivf Sperm Gradient KitCook Ob/Gyn2000—
−2K152782Sydney Ivf Sperm Medium, Sydney Ivf Sperm Gradient Kit, Sydney Ivf SpermientWilliam A. Cook Australia Pty., Ltd.2015—
−1K190199SepaSperm Washing Solution, SepaSperm SolutionKitazato Corporation2019—
0 (this device)K212410VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient MediumShenzhen Vitavitro Biotech Co., Ltd.2022—
+1K241095ARTSMedia Semen Wash MediumArtsmedia Denmark Aps2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K212410, 2000–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MQL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MQL device

  1. #1 K251305 Ultra-Fast Vitri; Ultra-Fast Warmscore 14.4 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K190199SepaSperm Washing Solution, SepaSperm Solution
Summary page 4
…Manufacturer Kitazato Corporation Predicate 510(k) No. K190199 Devices Regulatory Class Class II Product C…
Kitazato Corporation2019—

Also cleared against K190199: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K241095ARTSMedia Semen Wash MediumArtsmedia Denmark Aps20240

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 22 years and passes through 4 companies; a new generation was cleared every 3.8 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K241095 (Artsmedia Denmark Aps, 2024) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K190199.

How does its category compare?

All MQL devices

MQL Media, Reproductive: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · MQL

9in 2025

2007: 32008: 122009: 22010: 62011: 12012: 52014: 52015: 72016: 122017: 102018: 42019: 62020: 82021: 12022: 32023: 52024: 122025: 92026 (partial year): 3
2007high 12 (2008) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQL

225in 2025

2007: 212 days median2008: 151 days median2010: 235 days median2012: 253 days median2014: 142 days median2015: 87 days median2016: 170 days median2017: 113 days median2018: 94 days median2019: 170 days median2020: 257 days median2022: 316 days median2023: 199 days median2024: 195 days median2025: 225 days median2026 (partial year): 179 days median
2007high 316 (2022) · low 87 (2015)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MQL

1in 2023

2012: 12020: 12021: 22022: 12023: 1
2007high 2 (2021) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MQL

3in 2025

2012: 12013: 22014: 32016: 22023: 12024: 62025: 3
2007high 6 (2024) · low 0 (2007)2025

MAUDE reports naming product code MQL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007321200
20081215100
20092—00
2010623500
20111—00
2012525311
20130—02
2014514203
201578700
20161217002
20171011300
201849400
2019617000
2020825710
20211—20
2022331610
2023519911
20241219506
2025922503
202631790—

What is it indicated for?

VitaVitro® Sperm Washing Medium is intended for preparation and washing of sperm for use in assisted reproduction procedures. VitaVitro® Sperm Washing Medium is also intended for use in intrauterine insemination procedures.

VitaVitro® Sperm Gradient Medium is intended for separation of motile sperm from seminal fluid for use in assisted reproduction procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K212410: VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient Medium.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K212410

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026