Home › Device types › FGA
Kit, Nephroscope
FDA product code FGA · Class 2 · Gastroenterology, Urology
349
Registered devices
104
Adverse events
8
Recalls
10
510(k) clearances
Devices with this code
ClearPetra — Well Lead Medical Co.,Ltdn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGClearPetra — Well Lead Medical Co.,LtdNA — SCHÖLLY FIBEROPTIC GmbHClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdELECTROSURGICAL SNARE — OLYMPUS MEDICAL SYSTEMS CORP.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCSnare Wire — OLYMPUS MEDICAL SYSTEMS CORP.Olympus — OLYMPUS Winter & Ibe GmbHn.a. — Karl Storz GmbH & Co. KGCARDINAL HEALTH — Cardinal Health 200, LLCClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdCARDINAL HEALTH — Cardinal Health 200, LLCCOBRA VISION — Richard Wolf GmbHClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,Ltd
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
| 2024-07-23 | Karl Storz Endoscopy | Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA. |
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