FDA device listing

BNS R30C,BoneSTATION,FINEFIX MODULE KIT,FixSTATION,Histos-3, Histos-5, Histos-REM,Histos Series,KOS KIT HRW45/K,KOS…

FDA device listing 1732928923 · MILESTONE S.P.A.

Key facts

Proprietary names BNS R30C,BoneSTATION,FINEFIX MODULE KIT,FixSTATION,Histos-3, Histos-5, Histos-REM,Histos Series,KOS KIT HRW45/K,KOS, KOS-EM,KOS Series,LOGOS EVO,LOGOS, LOGOS J, LOGOS ONE,LOGOS ONE EVO,MAGNUS,Pathos, Pathos DELTA,Pathos Series,R24SM,RACK 48 CASSETTES,RB300,RHS-1, RHS-2, REM,RHS Series,STIRRING MODULE FOR EM 100-240V,SYNERGY KIT, BIOPSY MOLDS & PADS,SYNERGY KIT, STANDARD MOLDS & PADS
Owner/operator MILESTONE S.P.A.
Owner/operator number 10023724
Product codes IEO
Device names IEO - Processor, Tissue, Automated
Device class Class I
Classification regulations (21 CFR) 864.3875
Review panels Pathology
Registered establishments MILESTONE S.P.A.
Establishment registrations 1000391282
FEI numbers 1000391282
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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