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Dfix

Country not established

Dfix is a medical device manufacturer, with 8 devices listed in FDA GUDID (FDA Class I) as of 14 Nov 2026.

Devices
8

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 8
Device classes
  • FDA Class I 8
Identifiers
  • DUNS 695689958

What Dfix makes

DFIX manufactures devices for securing percutaneous catheters and tubes, including wearable holders and skin-closing tension systems. The SDFIX is designed for securing dialysis catheters, while the DIALFIX series (11, 15, 18, 21, 24, PLUS 3, PLUS 5) provides adjustable fixation for various tube sizes and medical applications.

All devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.

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

Catalogue8

Newest first, rows 1-8 of 8

Company details

DUNS number
695689958
Phone
+821027807692

Frequently asked questions

How many devices does DFIX have in the registry?

The registry currently lists 8 devices for DFIX. Devices recorded under merged duplicate company entries are counted once.

Which registries list DFIX's devices?

Among its 8 most recently registered devices, DFIX has devices listed in FDA GUDID (8 devices).

What risk classes do DFIX's devices fall under?

Among its 8 most recently registered devices, the classes recorded for DFIX's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from DFIX in the registry?

The most recently registered devices listed for DFIX include SDFIX 01, DIALFIX 11 01, DIALFIX 24 01 and DIALFIX PLUS 3 01.

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