Home › Device 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
Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Endo Catch Gold — Covidien LPKlein Surgical — Klein Surgical Systems, Inc.PEAK MEDICAL — Peak Medical Distribution Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Klein Surgical — Klein Surgical Systems, Inc.Endo Catch II — Covidien LP
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-05-12 | Covidien Llc | The 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 |
| 2020-05-12 | Covidien Llc | The 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 |
| 2020-05-12 | Covidien Llc | The 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 |
| 2020-05-12 | Covidien Llc | The 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 |
| 2015-02-11 | EXP Pharmaceutical Services Corp | EXP 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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
