Home › Device types › FGA
Kit, Nephroscope
FDA product code FGA · Class 2 · Gastroenterology, Urology
345
Registered devices
96
Adverse events
8
Recalls
10
510(k) clearances
Devices with this code
CARDINAL HEALTH — Cardinal Health 200, LLCELECTROSURGICAL KNIFE — OLYMPUS MEDICAL SYSTEMS CORP.n.a. — Karl Storz GmbH & Co. KGClearPetra — Well Lead Medical Co.,LtdPANOVIEW PLUS — Richard Wolf GmbHCARDINAL HEALTH — Cardinal Health 200, LLCClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdOlympus — OLYMPUS Winter & Ibe GmbHClearPetra — Well Lead Medical Co.,Ltdn.a. — Karl Storz GmbH & Co. KGClearPetra — Well Lead Medical Co.,Ltdn.a. — Karl Storz GmbH & Co. KGClearPetra — Well Lead Medical Co.,LtdCARDINAL HEALTH — Cardinal Health 200, LLCClearPetra — Well Lead Medical Co.,LtdOlympus — OLYMPUS Winter & Ibe GmbHPANOVIEW PLUS — Richard Wolf GmbHOES CYSTONEPHROFIBERSCOPE — OLYMPUS MEDICAL SYSTEMS CORP.Olympus — OLYMPUS Winter & Ibe GmbHClearPetra — Well Lead Medical Co.,LtdClearPetra — Well Lead Medical Co.,LtdCARDINAL HEALTH — Cardinal Health 200, LLCn.a. — Karl Storz GmbH & Co. KG
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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