Insufflation Retention Device (IRD) (11173-325-101)
K-Number: K261587 · 2026-07-02
Device Summary
Frequently Asked Questions
What is the Insufflation Retention Device (IRD) (11173-325-101)?
Insufflation Retention Device (IRD) (11173-325-101) is a medical device that received FDA 510(k) clearance on 2026-07-02. The listed applicant is BPEndo, LLC. The 510(k) number is K261587.
When did Insufflation Retention Device (IRD) (11173-325-101) receive FDA 510(k) clearance?
Insufflation Retention Device (IRD) (11173-325-101) received FDA 510(k) clearance on 2026-07-02, under 510(k) number K261587.
Who is the listed applicant for Insufflation Retention Device (IRD) (11173-325-101)?
The FDA 510(k) record lists BPEndo, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Insufflation Retention Device (IRD) (11173-325-101)?
The FDA product code for Insufflation Retention Device (IRD) (11173-325-101) is FDF.
Other records listing BPEndo, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FDF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.