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Endogator Kit

MEDIVATORS INC. · Model 4005471 · UDI-DI 40677964028104

OCX Prescription
1
510(k) clearances
271
Adverse events
18
Recalls
98
Facilities

Description

Endogator Kit includes Endogator Irrigation Tubing compatible with Boston Scientific Endostat II, Olympus OFP and Endo Stratus Irrigation Pump units, and Endo ENDO SMARTCAP Rinse and insufflation Tubing for PENTAX GI Endoscopes.

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.