510(k) Report

510(k) · Cleared

Cleared

Cryolock

K122982510(k) TraditionalCleared Jan 9, 2014470-day reviewClass II21 CFR 884.6160

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

Biotech, Inc. · MQK Labware, Assisted Reproduction

Cleared on Jan 9, 2014 as substantially equivalent to K041562 (Irvine Scientific Sales Co., Inc., 2004) and 1 other predicate after a 470-day review. Its family tree reaches back 2 generations to 2004. 8 later devices descend from it.

Decided
Jan 9, 2014
Review
470 days
Class
Class II
Product code
MQK
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K041562 (2004). 8 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2016: 2 descendants cleared2017: 2 descendants cleared2018: 3 descendants cleared2025: 1 descendant clearedK041562 · Cryotip · Irvine Scientific Sales Co., Inc. · 2004K090832 · Rapid-I · Vitrolife Sweden AB · 2009200020052010201520202025
Descendants, by generation 1 generation forward: 3 descendants2 generations forward: 4 descendants3 generations forward: 1 descendant K090832 · Rapid-I · Vitrolife Sweden AB · 2009K041562 · Cryotip · Irvine Scientific Sales Co., Inc. · 20040
  1. Root · 2 generations backK041562 CryotipIrvine Scientific Sales Co., Inc. · 2004
  2. 1 generation backK090832 Rapid-IVitrolife Sweden AB · 2009
  3. This deviceK122982 CryolockBiotech, Inc. · 2014
  4. Descendant · cites it directly · 3 of its ownK153027 Cryotop USKitazato Biopharma Co., Ltd. · 2016
  5. Descendant · 2 generations on · 1 of its ownK181469 Cryotop®US-flash and Cryotop®US-scoopKitazato Corporation · 2018
  6. Descendant · cites it directly · 1 of its ownK162640 iVitri EZReprobitech Corp. · 2017
  7. Descendant · cites it directly · 1 of its ownK162833 VitriGuardOrigio A/S · 2017 · Recalled
  8. Descendant · 3 generations on · 0 of its ownK241454 Minvitro® Vitrification Straw (MVT-VSN series, including MVT-VSNR…Guangzhou Hehong Biotech Co., Ltd. · 2025

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2016: 22017: 22018: 32025: 1
2016high 3 (2018) · low 0 (2019)2026

Most influential descendants

Showing 5 of 8 · See all
  • K153027Cryotop USKitazato Biopharma Co., Ltd. · 2016 · cites it directly3descendants
  • K181469Cryotop®US-flash and Cryotop®US-scoopKitazato Corporation · 2018 · 2 generations on1descendant
  • K162640iVitri EZReprobitech Corp. · 2017 · cites it directly1descendant
  • K162833VitriGuardOrigio A/S · 2017 · cites it directly1descendant
  • K241454Minvitro® Vitrification Straw (MVT-VSN series, including MVT-VSNR, MVT-VSNY, MVT-VSNB…Guangzhou Hehong Biotech Co., Ltd. · 2025 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K041562CryotipIrvine Scientific Sales Co., Inc.2004—
−1K090832Rapid-IVitrolife Sweden AB2009—
0 (this device)K122982CryolockBiotech, Inc.2014—
+1K153027Cryotop USKitazato Biopharma Co., Ltd.2016—
+2K181469Cryotop®US-flash and Cryotop®US-scoopKitazato Corporation2018—
+1K162640iVitri EZReprobitech Corp.2017—
+1K162833VitriGuardOrigio A/S20171
+3K241454Minvitro® Vitrification Straw (MVT-VSN series, including MVT-VSNR, MVT-VSNY…Guangzhou Hehong Biotech Co., Ltd.2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201620
201720
201830
202510
FIG. 1 — Lineage of K122982, 2004–2025Source: 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 MQK? 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 MQK device

  1. #1 K241626 SperSort™ Sperm Sorting Chip (IPG02)score 10.1 · 5 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? (2)

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
*K041562Cryotip
Summary page 1
…Assisted Reproduction Labware Regulation 884.6160 Product Code MQK Predicate HSV Straw K04 1562 Rapid-I K090832 Description The CRYOLOCK TM is a cryopreservation storage devic…
Irvine Scientific Sales Co., Inc.2004—
*K090832Rapid-I
Summary page 1
…884.6160 Product Code MQK Predicate HSV Straw K04 1562 Rapid-I K090832 Description The CRYOLOCK TM is a cryopreservation storage device that is intended for use in vitrification procedur…
Vitrolife Sweden AB2009—

Also cleared against K041562: 3 other devices →

What descends from it? (8)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K153027Cryotop USKitazato Biopharma Co., Ltd.20163
K162640iVitri EZReprobitech Corp.20171
K162833VitriGuardOrigio A/S20171

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 10 years and passes through 3 companies; a new generation was cleared every 5.4 years on median.
  • None of the 2 ancestors has a recall.
  • Of its descendants, K153027 (Kitazato Biopharma Co., Ltd., 2016) has gone furthest, with 3 descendants of its own.
  • 3 other devices also cite its predicate K041562.

How does its category compare?

All MQK devices

MQK Labware, Assisted Reproduction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · MQK

3in 2025

2007: 12008: 22009: 22010: 22011: 12012: 32013: 12014: 62015: 22016: 22017: 22018: 42019: 12020: 22021: 12022: 22024: 42025: 32026 (partial year): 1
2007high 6 (2014) · low 0 (2023)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQK

259in 2025

2012: 454 days median2014: 270 days median2018: 154 days median2024: 163 days median2025: 259 days median
2007high 454 (2012) · low 154 (2018)2026

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

Recalls per year · MQK

1in 2011

2007: 12011: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · MQK

1in 2025

2025: 1
2007high 1 (2025) · low 0 (2007)2025

MAUDE reports naming product code MQK, 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
20071—10
20082—00
20092—00
20102—00
20111—10
2012345400
20131—00
2014627000
20152—00
20162—00
20172—00
2018415400
20191—00
20202—00
20211—00
20222—00
20230—00
2024416300
2025325901
20261—0—

What is it indicated for?

The CRYOLOCK T5' is a cryopreservation storage device that is intended for use in vitrification procedures to contain and maintain human 1-cell stage embryos.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122982: Cryolock.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122982

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