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Ingestible Event Marker

FDA product code OZW · Class 2 · General Hospital

27
Registered devices
2
Adverse events
0
Recalls
8
510(k) clearances

Devices with this code

NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.Proteus Digital Health Feedback System — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.Proteus Digital Health Feedback System — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.Proteus Digital Health Feedback System — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.Proteus Digital Health Feedback System — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.NA — PROTEUS DIGITAL HEALTH, INC.

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