FDA Device Intelligence
HomeDevice types › GCI

Laryngoscope, Endoscope

FDA product code GCI · Class 2 · Gastroenterology, Urology

19
Registered devices
1,664
Adverse events
5
Recalls
14
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-05-12Covidien LlcThe product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instru
2020-05-12Covidien LlcThe product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instru
2020-05-12Covidien LlcThe product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instru
2020-05-12Covidien LlcThe product is recalled due to a manufacturing assembly error that may cause the staples to fail to properly advance within the staple cartridge when the instru
2015-02-11EXP Pharmaceutical Services CorpEXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.