510(k) Report

510(k) · Cleared

Cleared

Midas Rex Motors (Midas I, II & Convertible Models)

K952300510(k) TraditionalCleared May 26, 199510-day reviewClass I21 CFR 878.4820

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

Midas Rex Pneumatic Tools, Inc. · GET Motor, Surgical Instrument, Pneumatic Powered

Cleared on May 26, 1995 after a 10-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 2 later devices descend from it.

Decided
May 26, 1995
Review
10 days
Class
Class I
Product code
GET
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared1997: 1 descendant cleared1995200020052010201520202025
  1. This deviceK952300 Midas Rex Motors (Midas I, II & Convertible Models)Midas Rex Pneumatic Tools, Inc. · 1995
  2. Descendant · cites it directly · 1 of its ownK962483 Midas Rex Iii MotorMidas Rex Pneumatic Tools, Inc. · 1996
  3. Descendant · 2 generations on · 0 of its ownK970965 Midas Rex Iii Motor and Attachments (Midas Iii)Midas Rex Pneumatic Tools, Inc. · 1997

Most influential descendants

Showing 2 of 2 · See all
  • K962483Midas Rex Iii MotorMidas Rex Pneumatic Tools, Inc. · 1996 · cites it directly1descendant
  • K970965Midas Rex Iii Motor and Attachments (Midas Iii)Midas Rex Pneumatic Tools, Inc. · 1997 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K952300Midas Rex Motors (Midas I, II & Convertible Models)Midas Rex Pneumatic Tools, Inc.1995—
+1K962483Midas Rex Iii MotorMidas Rex Pneumatic Tools, Inc.1996—
+2K970965Midas Rex Iii Motor and Attachments (Midas Iii)Midas Rex Pneumatic Tools, Inc.1997—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
FIG. 1 — Lineage of K952300, 1995–1997Source: 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 GET? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K962483Midas Rex Iii MotorMidas Rex Pneumatic Tools, Inc.19961

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, K962483 (Midas Rex Pneumatic Tools, Inc., 1996) has gone furthest, with 1 descendant of its own.

How does its category compare?

All GET devices

GET Motor, Surgical Instrument, Pneumatic Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GET

FDA has decided no GET device since 2007.

Median 510(k) review, days · GET

Too few GET 510(k)s in any year since 2007 to give a median.

Recalls per year · GET

1in 2013

2008: 472013: 1
2007high 47 (2008) · low 0 (2007)2026

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

Adverse event reports per year · GET

8in 2025

2007: 332008: 82009: 112010: 352011: 2802012: 482013: 342014: 262015: 432016: 292017: 452018: 462019: 152020: 152021: 92022: 132023: 62024: 192025: 8
2007high 280 (2011) · low 6 (2023)2025

MAUDE reports naming product code GET, 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—033
20080—478
20090—011
20100—035
20110—0280
20120—048
20130—134
20140—026
20150—043
20160—029
20170—045
20180—046
20190—015
20200—015
20210—09
20220—013
20230—06
20240—019
20250—08
20260—0—

More from Midas Rex Pneumatic Tools, Inc.

12 FDA decisions under this applicant name. See the company

  • K972289Midas Rex MotorMidas Rex Pneumatic Tools, Inc. · 1997
  • K970965Midas Rex Iii Motor and Attachments (Midas Iii)Midas Rex Pneumatic Tools, Inc. · 1997
  • K962483Midas Rex Iii MotorMidas Rex Pneumatic Tools, Inc. · 1996
  • K953434Midas Rex Motors, (Midas I, Midas II & Convertible Models)Midas Rex Pneumatic Tools, Inc. · 1996
  • K954076Midas Rex Drill Attachments & Twist DrillsMidas Rex Pneumatic Tools, Inc. · 1995

Recent decisions in GET

The GET category page

  • K960473Aesculap Power System HandpieceAesculap, Inc. · 1996
  • K955174Sodem High Speed System for Neurosurgery & Median StyernotomySodem Diffusion SA · 1996
  • K942987Nucleotome L KitSurgical Dynamics, Inc. · 1995
  • K954076Midas Rex Drill Attachments & Twist DrillsMidas Rex Pneumatic Tools, Inc. · 1995
  • K953433Midas Rex Telescoping SystemMidas Rex Pneumatic Tools, Inc. · 19952 recalls

https://510kreport.com/device/K952300 · printed Nov 6, 2026

Cite this page

510(k) Report. “K952300: Midas Rex Motors (Midas I, II & Convertible Models).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K952300

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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