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Probe And Director, Gastro-Urology
FDA product code FGM · Class 1 · Gastroenterology, Urology
307
Registered devices
20
Adverse events
1
Recalls
7
510(k) clearances
Devices with this code
AESCULAP — AESCULAP, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHGimmi — Gimmi GmbHIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONNA — Richard Wolf GmbHIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHV. Mueller — STERIS CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMillennium — Avalign Technologies, Inc.V. Mueller — STERIS CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMillennium — Avalign Technologies, Inc.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHMillennium — Avalign Technologies, Inc.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHLOCKHART MUMMERY FISTULA PROBE — SONTEC INSTRUMENTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-02-06 | Medtronic Gastroenterology / Urology | The product's rear panel label could smear during use causing the serial number to be unreadible. This has the remote possibility of resulting in patient data |
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