510(k) Report

510(k) · Cleared

Cleared

Porges Dormia 3 FR Flat Wire Basket Stone Dislodge

K900269510(k) TraditionalCleared Jul 3, 1990166-day reviewClass II21 CFR 876.4680

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

Porges Corp. · FFL Dislodger, Stone, Basket, Ureteral, Metal

Cleared on Jul 3, 1990 after a 166-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Jul 3, 1990
Review
166 days
Class
Class II
Product code
FFL
Recalls
None
Predicates
0

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

FIG. 1 — Lineage of K900269Source: 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.

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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 FFL devices

FFL Dislodger, Stone, Basket, Ureteral, Metal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FFL

1in 2019

2008: 12011: 12017: 12019: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FFL

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

Recalls per year · FFL

1in 2022

2008: 12014: 12022: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · FFL

496in 2025

2007: 682008: 1522009: 1942010: 1922011: 1292012: 952013: 982014: 712015: 792016: 882017: 5172018: 4282019: 3512020: 3752021: 3582022: 4262023: 5932024: 6062025: 496
2007high 606 (2024) · low 68 (2007)2025

MAUDE reports naming product code FFL, 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—068
20081—1152
20090—0194
20100—0192
20111—0129
20120—095
20130—098
20140—171
20150—079
20160—088
20171—0517
20180—0428
20191—0351
20200—0375
20210—0358
20220—1426
20230—0593
20240—0606
20250—0496
20260—0—
Cite this page

510(k) Report. “K900269: Porges Dormia 3 FR Flat Wire Basket Stone Dislodge.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K900269

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