510(k) Report

510(k) · Cleared

Cleared

MTG - Minitub Heated Stage Systems

K002971510(k) TraditionalCleared Dec 15, 200084-day reviewClass II21 CFR 884.6120

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

Zander Medical Supplies, Inc. · MQG Accessory, Assisted Reproduction

Cleared on Dec 15, 2000 after an 84-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Dec 15, 2000
Review
84 days
Class
Class II
Product code
MQG
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2012: 1 descendant cleared200020052010201520202025
  1. This deviceK002971 MTG - Minitub Heated Stage SystemsZander Medical Supplies, Inc. · 2000
  2. Descendant · cites it directly · 0 of its ownK112644 Seaforia Sperm Separation Assistance SystemLotus Bio, Ltd. · 2012

Most influential descendants

Showing 1 of 1 · See all
  • K112644Seaforia Sperm Separation Assistance SystemLotus Bio, Ltd. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K002971MTG - Minitub Heated Stage SystemsZander Medical Supplies, Inc.2000—
+1K112644Seaforia Sperm Separation Assistance SystemLotus Bio, Ltd.2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K002971, 2000–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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

Planning a device in MQG? 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 MQG device

  1. #1 K261083 Wallace® Aspiration Pump (WAPV1); Wallace®…score 12.2 · 2 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K112644Seaforia Sperm Separation Assistance SystemLotus Bio, Ltd.20120

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?

  • Of its descendants, K112644 (Lotus Bio, Ltd., 2012) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MQG devices

MQG Accessory, Assisted Reproduction: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MQG

1in 2025

2011: 42012: 12014: 32016: 22017: 22018: 32024: 12025: 12026 (partial year): 2
2007high 4 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQG

135in 2018

2011: 137 days median2014: 236 days median2018: 135 days median
2007high 236 (2014) · low 135 (2018)2026

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

Recalls per year · MQG

1in 2023

2019: 12020: 12023: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · MQG

1in 2025

2016: 12019: 22020: 32023: 32024: 12025: 1
2007high 3 (2020) · low 0 (2007)2025

MAUDE reports naming product code MQG, 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
20070—00
20080—00
20090—00
20100—00
2011413700
20121—00
20130—00
2014323600
20150—00
20162—01
20172—00
2018313500
20190—12
20200—13
20210—00
20220—00
20230—13
20241—01
20251—01
20262—0—
Cite this page

510(k) Report. “K002971: MTG - Minitub Heated Stage Systems.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K002971

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026