510(k) Report

510(k) · Cleared

Cleared

OB Tripp Transport Chair

K823151510(k) TraditionalCleared Nov 5, 198216-day reviewClass I21 CFR 890.3100

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

Orthion Corp. · INM Chair, With Casters

Cleared on Nov 5, 1982 after a 16-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Nov 5, 1982
Review
16 days
Class
Class I
Product code
INM
Recalls
None
Predicates
0

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

FIG. 1 — Lineage of K823151Source: FDA 510(k) database · 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 INM? 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 has not posted a summary or statement for it, so its predicates are not known.

What descends from it?

No later submission names this one as a predicate yet.

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.

How does its category compare?

All INM devices

INM Chair, With Casters: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · INM

1in 2007

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

2026 to Oct 25, outlined.

Median 510(k) review, days · INM

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

Recalls per year · INM

1in 2021

2010: 12011: 32012: 112017: 12021: 1
2007high 11 (2012) · low 0 (2007)2026

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

Adverse event reports per year · INM

15in 2025

2007: 122008: 132009: 122010: 102011: 492012: 1752013: 4632014: 6772015: 152016: 182017: 82018: 112019: 132020: 92021: 222022: 112023: 112024: 82025: 15
2007high 677 (2014) · low 8 (2017)2025

MAUDE reports naming product code INM, 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—012
20080—013
20090—012
20100—110
20110—349
20120—11175
20130—0463
20140—0677
20150—015
20160—018
20170—18
20180—011
20190—013
20200—09
20210—122
20220—011
20230—011
20240—08
20250—015
20260—0—

More from Orthion Corp.

11 FDA decisions under this applicant name. See the company

  • K832546Mark V High Voltage Galvanic StimulatorrOrthion Corp. · 1983
  • K823149OB Tilt TableOrthion Corp. · 1982
  • K823153Bath Tub Seat & Bath BoardOrthion Corp. · 1982
  • K823156Collapsable Lavatory HeightenerOrthion Corp. · 1982
  • K823150Sesam Treatment TableOrthion Corp. · 1982

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https://510kreport.com/device/K823151 · printed Nov 4, 2026

Cite this page

510(k) Report. “K823151: OB Tripp Transport Chair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K823151

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