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Device, Acupressure

FDA product code MVV · Class U · Unknown

18
Registered devices
5
Adverse events
1
Recalls
13
510(k) clearances

Devices with this code

Sea-Band — SEA-BAND LIMITEDFrida — Fridababy, LLCSea-Band — SEA-BAND LIMITEDTumEase — MUMEASE LLCTumEase — MUMEASE LLCWALGREENS — WALGREEN CO.RITEAID — RITE AID CORPORATIONSea-Band — SEA-BAND LIMITEDTumEase — MUMEASE LLCCORE VALUES — APOTHECARY PRODUCTS, LLCFlents — APOTHECARY PRODUCTS, LLCMumEase — MUMEASE LLCAcu-Life (HE) — APOTHECARY PRODUCTS, LLCTumEase — MUMEASE LLCTumEase — MUMEASE LLCCVS Health — WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDTumEase — MUMEASE LLCSea-Band — SEA-BAND LIMITED

Recent recalls

DateFirmReason
2007-04-26Psi Health SolutionsProduct was marketed before its 510(k) application cleared.

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