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Anoscope And Accessories

FDA product code FER · Class 2 · Gastroenterology, Urology

190
Registered devices
86
Adverse events
1
Recalls
27
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-12-12Applied Medical Resources CorpUnintentional shifting of the tip insulation of the firm's electrosurgical probes.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.