510(k) Report

510(k) · Cleared

Cleared

Harmony Latex Dam, Harmony Non-Latex Dam

K203727510(k) TraditionalCleared Aug 5, 2021227-day reviewClass II21 CFR 884.5300

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

Pamco Distributing, Inc. · MSC Barrier, Std, Oral Sex

Cleared on Aug 5, 2021 as substantially equivalent to K091769 (Line One Laboratories, Inc., 2010) after a 227-day review. Its family tree reaches back 2 generations to 1999.

Decided
Aug 5, 2021
Review
227 days
Class
Class II
Product code
MSC
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K990067 (1999). No later device cites it as a predicate yet.

  1. Root · 2 generations backK990067 Sheer Glyde DamsLouise C. Myers · 1999
  2. 1 generation backK091769 Trust DamLine One Laboratories, Inc. · 2010
  3. This deviceK203727 Harmony Latex Dam, Harmony Non-Latex DamPamco Distributing, Inc. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K990067Sheer Glyde DamsLouise C. Myers1999—
−1K091769Trust DamLine One Laboratories, Inc.2010—
0 (this device)K203727Harmony Latex Dam, Harmony Non-Latex DamPamco Distributing, Inc.2021—
FIG. 1 — Lineage of K203727, 1999–2021Source: 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), 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 MSC? 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 MSC device

  1. #1 K253662 Lixi (LXOSFM1)score 12.3 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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
*K091769Trust Dam
Summary page 4
…CFR 884.5300 Regulation Name: Condom Regulatory Class: Class II Product Code: MSC (Barrier, Std, Oral Sex) Predicate Device Trust Dam (K091769) The predicate has not been subject to a design-related recall. Indications for Use The Harmony® Latex & the Harmony® Polyiso…
Line One Laboratories, Inc.2010—

Also cleared against K091769: 2 other devices →

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.

What does this lineage say?

  • The line of descent spans 22 years and passes through 3 companies; a new generation was cleared every 11.5 years on median.
  • None of the 2 ancestors has a recall.
  • 2 other devices also cite its predicate K091769.

How does its category compare?

All MSC devices

MSC Barrier, Std, Oral Sex: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · MSC

2in 2022

2010: 12021: 12022: 22026 (partial year): 1
2007high 2 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSC

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

Recalls per year · MSC

No recall names MSC since 2007.

Adverse event reports per year · MSC

No MAUDE report names MSC since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20101—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20211—00
20222—00
20230—00
20240—00
20250—00
20261—0—

What is it indicated for?

The Harmony® Latex & the Harmony® Polyisoprene Dams are used as a barrier when engaging in oral/vaginal and oral/anal sex to help reduce the transmission of bodily fluids, harmful pathogens and sexually transmitted infections.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K203727: Harmony Latex Dam, Harmony Non-Latex Dam.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K203727

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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