Insufflation Retention Device (IRD) (11173-325-101)— 510(k) K261587

Name: FDA 510(k) clearance K261587
Creator: U.S. Food and Drug Administration
Published: 2026-07-02

Substantially Equivalent

BPEndo, LLC

FDA 510(k) clearance K261587 for Insufflation Retention Device (IRD) (11173-325-101), Substantially Equivalent on 2026-07-02. Applicant: BPEndo, LLC. Device class: 2.

Clearance details

Applicant: BPEndo, LLC
Product code: Code FDF
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2026-05-13
Decision date: 2026-07-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Norman, OK, US

Download summary PDF View on FDA.gov ↗

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K213773 — Insufflation Retention Device2022-07-21

Adverse events under product code FDF

product code FDF

Death: 8
Injury: 729
Malfunction: 61,773
Total: 62,510

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.