CALYXO, INC.
1 recall(s) on record — most severe on record: Class I.
Activity by year
- Recalls (1)
Devices registered here (2)
- Ureteroscope And Accessories, Flexible/RigidProduct code FGB (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.1500
- Endoscopic Access Overtube, Gastroenterology-UrologyProduct code FED (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.1500
Recalls & enforcement
- Class IOngoing2025-02-19Aspiration system, for endoscopic examination/treatment of urinary tract and kidney interior, to have labeling update adding additional instructions, for patients with high viscosity fluid in the kidney, not to continue providing fluid inflow in the presence of unresolved slow or…
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “CALYXO, INC. (FEI 3032959393) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3032959393-calyxo-inc/
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