510(k) Report

510(k) · Cleared

Cleared

Lubricant, Otrho Personal

K790087510(k) TraditionalCleared Feb 1, 197915-day reviewClass I21 CFR 880.6375

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

Ortho Pharmaceutical Corp. · KMJ Lubricant, Patient

Cleared on Feb 1, 1979 after a 15-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
Feb 1, 1979
Review
15 days
Class
Class I
Product code
KMJ
Recalls
None
Predicates
0

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

Descendants, by year cleared 1997: 1 descendant cleared19801990200020102020
  1. This deviceK790087 Lubricant, Otrho PersonalOrtho Pharmaceutical Corp. · 1979
  2. Descendant · cites it directly · 0 of its ownK973780 Personal Lubricating LiquidQualis, Inc. · 1997

Most influential descendants

Showing 1 of 1 · See all
  • K973780Personal Lubricating LiquidQualis, Inc. · 1997 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K790087Lubricant, Otrho PersonalOrtho Pharmaceutical Corp.1979—
+1K973780Personal Lubricating LiquidQualis, Inc.1997—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
FIG. 1 — Lineage of K790087, 1979–1997Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KMJ? 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
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
K973780Personal Lubricating LiquidQualis, Inc.19970

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, K973780 (Qualis, Inc., 1997) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KMJ devices

KMJ Lubricant, Patient: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KMJ

1in 2015

2008: 32009: 12010: 12011: 12012: 32013: 12014: 12015: 1
2007high 3 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KMJ

141in 2012

2008: 86 days median2012: 141 days median
2007high 141 (2012) · low 86 (2008)2026

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

Recalls per year · KMJ

1in 2016

2010: 12011: 122016: 1
2007high 12 (2011) · low 0 (2007)2026

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

Adverse event reports per year · KMJ

1in 2025

2007: 52008: 32009: 12010: 12011: 72012: 22013: 62014: 22015: 42016: 52017: 12018: 52019: 22020: 12022: 42023: 42024: 32025: 1
2007high 7 (2011) · low 0 (2021)2025

MAUDE reports naming product code KMJ, 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—05
200838603
20091—01
20101—11
20111—127
2012314102
20131—06
20141—02
20151—04
20160—15
20170—01
20180—05
20190—02
20200—01
20210—00
20220—04
20230—04
20240—03
20250—01
20260—0—
Cite this page

510(k) Report. “K790087: Lubricant, Otrho Personal.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K790087

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
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026