FDA Device Intelligence
HomeDevice types › ILJ

Bath, Hydro-Massage

FDA product code ILJ · Class 2 · Physical Medicine

925
Registered devices
1,022
Adverse events
10
Recalls
73
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.
2025-08-13Penner Patient Care, Inc.The device does not bear a unique device identifier.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.