510(k) Report

510(k) · Cleared

Cleared

CyClean Cord

K254239510(k) TraditionalCleared Mar 27, 202688-day reviewClass U

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

SS Global · MVL Cord, Retraction

Cleared on Mar 27, 2026 as substantially equivalent to K171577 (Eastdent Co., Ltd., 2018) after an 88-day review. Its family tree reaches back 2 generations to 2013.

Decided
Mar 27, 2026
Review
88 days
Class
Class U
Product code
MVL
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K132526 (2013). No later device cites it as a predicate yet.

  1. Root · 2 generations backK132526 Knit-Pak+Premier Dental Products Co. · 2013
  2. 1 generation backK171577 Smartcord, Smartcord XEastdent Co., Ltd. · 2018
  3. This deviceK254239 CyClean CordSS Global · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K132526Knit-Pak+Premier Dental Products Co.2013—
−1K171577Smartcord, Smartcord XEastdent Co., Ltd.2018—
0 (this device)K254239CyClean CordSS Global2026—
FIG. 1 — Lineage of K254239, 2013–2026Source: 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 MVL? 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 MVL device

  1. #1 K253797 One-Stopscore 11.2 · 2 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
*K171577Smartcord, Smartcord X
Summary page 5
…Classification Name: Retraction Cord • Product Code: MVL • Classification regulation: Unclassified 4. Predicate Device: Smartcord X by EASTDENT CO., LTD. (K171577) 5. Description: The CyClean Cord is a dental gingival retraction cord containing aluminum chloride Hexahydrate in 100% l…
Eastdent Co., Ltd.2018—

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 13 years and passes through 3 companies; a new generation was cleared every 7.9 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All MVL devices

MVL Cord, Retraction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · MVL

1in 2025

2008: 12009: 32010: 42011: 22012: 12013: 22014: 22015: 22017: 42018: 12019: 12020: 22021: 12022: 22025: 12026 (partial year): 2
2007high 4 (2010) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MVL

227in 2017

2009: 91 days median2010: 79 days median2017: 227 days median
2007high 227 (2017) · low 79 (2010)2026

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

Recalls per year · MVL

1so far in 2026, the most since 2007

2026 (partial year): 1
2007high 1 (2026) · low 0 (2007)2026

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

Adverse event reports per year · MVL

1in 2025

2009: 12010: 12012: 72013: 52014: 22021: 32022: 12024: 12025: 1
2007high 7 (2012) · low 0 (2007)2025

MAUDE reports naming product code MVL, 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
20081—00
200939101
201047901
20112—00
20121—07
20132—05
20142—02
20152—00
20160—00
2017422700
20181—00
20191—00
20202—00
20211—03
20222—01
20230—00
20240—01
20251—01
20262—1—

What is it indicated for?

CyClean Cord is knitted retraction cord made from 100% lyocell, impregnated with Aluminum Chloride Hexahydrate for the temporary gingival retraction and hemostasis of the gingival margin.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K254239: CyClean Cord.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K254239

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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