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Reveal

US Endoscopy · Model 00711774 · UDI-DI 00816765012697

OCX Prescription
10
510(k) clearances
261
Adverse events
18
Recalls
98
Facilities

Description

The Reveal distal attachment cap is attached to the distal end of the endoscope to facilitate endoscopic therapy. The Reveal distal attachment cap is intended for the following: gastrointestinal mucosal resection (endoscopic mucosal resection) and keeping the suitable depth of endoscope's view field.

Recalls

DateFirmReason
2026-03-31Erbe Medical, LLCDevices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl
2026-03-31Erbe Medical, LLCDevices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl
2022-07-29Hobbs Medical, Inc.Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration
2022-07-29Hobbs Medical, Inc.Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
2020-11-03GA HEALTH COMPANY LIMITEDSuction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.