FDA device listing

ACGOV ADVANCED,ACGOV BASIC,ACTIVECARE 36 ADJUST,ACTIVECARE 36 DELUXE,ACTIVECARE 36 FIXED,ACTIVECARE 42 ADJUST,ACTIVECARE…

FDA device listing 1607340390 · MED-MIZER, INC

Key facts

Proprietary names ACGOV ADVANCED,ACGOV BASIC,ACTIVECARE 36 ADJUST,ACTIVECARE 36 DELUXE,ACTIVECARE 36 FIXED,ACTIVECARE 42 ADJUST,ACTIVECARE 42 DELUXE,ACTIVECARE 42 FIXED,ALLCARE,ALLCARE-C,CC803,COMFORTWIDE,EX5000A,EX5000C,EX6000,EX8000,EX8000-LC,MedSurg,PR1000,PR1000DS,PR8000,PR8000DS,RETRACT-F,RETRACT-V,RV6,SELECTCARE,SS763,SS763A,SS803,SS803A
Owner/operator MED-MIZER, INC
Owner/operator number 9057047
Product codes FNL
Device names FNL - Bed, Ac-Powered Adjustable Hospital
Device class Class II
Classification regulations (21 CFR) 880.5100
Review panels General Hospital
Registered establishments MED-MIZER, INC
Establishment registrations 3004976058
FEI numbers 3004976058
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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