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Amicon, Inc.

United StatesFDA applicant, unverified

Devices
20

What Amicon, Inc. makes

Amicon, Inc. manufactures ultrafiltration devices for blood processing, including concentrator systems like the MINICON CONCENTRATOR and CENTRIPREP CONCENTRATOR, as well as hemofilters such as the AMICON MINIFILTER PLUS HEMOFILTER and DIAFILTER 20 & 30 HEMOFILTERS. Their portfolio also includes systems like the MULTI-CELL ULTRAFILTRATION SYSTEM and micropartition devices like the CENTRIFREE MICROPARTITION SYSTEM, designed for blood component separation and purification.

These devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue20

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  • Minicon Concentrator Ref K760592

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Amicon Minifilter Plus Hemofilter Ref K895405

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Amicon Diafilters 20 & 30 Hemofilters Ref K823288

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Amicon Hemoconcentrator Set Ref K901286

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Centriprep 100 Ref K900280

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Minifilter Hemofilter Ref K853510

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hemofilters Ref K813591

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Minicon Ref K770398

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Multi-Cell Ultrafiltration System Ref K761100

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Amicon Diafilter Hemofilter Ref K863823

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Centriprep Concentrator Ref K870690

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Centrifree Micropartition System Ref K820455

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Amicon Equaline Fluid Balance System Ref K875121

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Centricon Concentrator Ref K893733

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Amicon Diafilter 30 Hemoconcentrator Ref K902837

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Amicon Ultrafiltration Membranes Cmii Ref K810810

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Centricon Micro-Concentrator Ref K833919

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Centricon -50 Concentrator Ref K930168

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Arteriovenous Blood Tubing Set For Ref K823881

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Amicon Vitafiber Flo-Path Biorect/Vls Cell Cult Sy Ref K892645

    Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 1-20 of 20

Frequently asked questions

How many devices does Amicon, Inc. have in the registry?

The registry currently lists 20 devices for Amicon, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Amicon, Inc.'s devices?

Among its 20 most recently registered devices, Amicon, Inc. has devices listed in FDA 510(k) (20 devices).

What risk classes do Amicon, Inc.'s devices fall under?

Among its 20 most recently registered devices, the classes recorded for Amicon, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Amicon, Inc. in the registry?

The most recently registered devices listed for Amicon, Inc. include MINICON CONCENTRATOR, AMICON MINIFILTER PLUS HEMOFILTER, AMICON DIAFILTERS 20 & 30 HEMOFILTERS and AMICON HEMOCONCENTRATOR SET.

Generated automatically from registry data and not verified by a human reviewer.