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Kaneka Corp.

Active in EUDAMED

Registered as KANEKA Corporation in EUDAMED

Japanfrom SRN EUDAMED SRN JP-MF-000022143

Part of KANEKA Corporation

Devices
1,489
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Kaneka Corp. makes

Kaneka Corp. manufactures a range of interventional and vascular devices, including coronary and peripheral angioplasty balloon catheters for clearing blocked arteries, embolization coils for treating vascular abnormalities, and thrombectomy suction catheters for removing clots. Their portfolio also includes lacrimal tubes for drainage of the tear duct, electronic vascular implant detachers for retrieving devices post-deployment, and haemoperfusion absorption columns for filtering toxins from blood.

The company’s devices are classified under FDA’s Class II, Unclassified, and Class U categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Kaneka Corp. is based in the United States, adhering to regulatory requirements for medical devices in that jurisdiction.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1,489

Newest first, rows 1-50 of 1,489

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  • Ed Coil Ref 353-03H6R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 350-0620RS

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • i-ED COIL 392-0615

    Active Regimes: 510(k) Registry: GUDID Class:II
  • i-ED COIL 392-0720

    Active Regimes: 510(k) Registry: GUDID Class:II
  • i-ED COIL 393-020320

    Active Regimes: 510(k) Registry: GUDID Class:II
  • i-ED COIL 393-020330

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Ed Coil Ref 353-0406

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0206

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0306RS

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0303

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0303R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 350-0606R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 350-0720

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0304RS

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 350-1215R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-01H2RS

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 350-0505R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 352-1610R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 352-0306

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 350-1220R

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0408RS

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 353-0510

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Ed Coil Ref 352-0308

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Rx Takeru Dc-RY4515UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • i-ED COIL 372-041030

    Listed Registry: GUDID Class:II
  • Rx Takeru Dc-RY3712UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Rx Takeru Dc-RY3510UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lacriflow Cl Lf-CL105A

    Active Regimes: 510(k) Registry: GUDID Class:—
  • i-ED COIL 393-020304

    Listed Registry: GUDID Class:II
  • Crosstella Rx Bd-F60060ER

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Rx Takeru Dc-RY4512UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • i-ED COIL 390-01H2

    Listed Registry: GUDID Class:II
  • Otw Takeru Dc-PY3215UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Crosstella Rx Bd-F30040ER

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Crosstella Rx Bd-F25150ER

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Otw Takeru Dc-PY5008UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • i-ED COIL 390-0101

    Listed Registry: GUDID Class:II
  • Crosstella Rx Bd-F30060ER

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Otw Takeru Dc-PY4515UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Crosstella Rx Bd-F20200ER

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Crosstella Rx Bd-F30100ER

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Otw Takeru Dc-PY5015UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Rx Takeru Dc-RY2508UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Lixelle S-35

    Active Regimes: HDE Registry: GUDID Class:—
  • i-ED COIL 390-0304

    Listed Registry: GUDID Class:II
  • i-ED COIL 373-040815

    Listed Registry: GUDID Class:II
  • Rx Takeru Dc-RY2008UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Rx Takeru Dc-RY2020UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Rx Takeru Dc-RY3220UA2

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Rx Nc Takeru Dc-RZ2721UA2

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

Rows 1-50 of 1,489

Showing 1-50 of 1,489

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
JP-MF-000022143
EUDAMED status
Active
EUDAMED registered name
KANEKA Corporation
Registered address
3-18, 2-chome Nakanoshima, 530-8288, Osaka-city, Japan
Phone
+815031339235
PRRC contact
Kazuaki Sanaka(public in EUDAMED)

Frequently asked questions

How many devices does Kaneka Corp. have in the registry?

The registry currently lists 1489 devices for Kaneka Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kaneka Corp.'s devices?

Among its 50 most recently registered devices, Kaneka Corp. has devices listed in EUDAMED (19 devices) and FDA GUDID (31 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Kaneka Corp.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Kaneka Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Kaneka Corp. in the registry?

The most recently registered devices listed for Kaneka Corp. include ED COIL, i-ED COIL 392-0615, i-ED COIL 392-0720 and i-ED COIL 393-020320.

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