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Asia Dynamics, Inc.

United StatesFDA applicant, unverified

Devices
4

What Asia Dynamics, Inc. makes

Asia Dynamics, Inc. manufactures single-use medical devices including a catheter with an integrated valve for fluid management, non-sterile latex examination gloves, sterile gauze sponges for wound care, and the Hemo-Barrier, a barrier device for medical procedures.

The company’s portfolio includes devices classified as Class I, Class II, and unclassified (U) under FDA regulations, with relevant products listed via the 510(k) pathway. The manufacturer operates in the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

  • Adi Catheter With Valve Ref K952924

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Mic Non-Sterile Latex Gloves Ref K891160

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Adi Sterile Gauze Sponges Ref K953501

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Hemo-Barrier Ref K953500

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

Frequently asked questions

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

The registry currently lists 4 devices for Asia Dynamics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Asia Dynamics, Inc.'s devices?

Among its 4 most recently registered devices, Asia Dynamics, Inc. has devices listed in FDA 510(k) (4 devices).

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

Among its 4 most recently registered devices, the classes recorded for Asia Dynamics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Asia Dynamics, Inc. include ADI CATHETER WITH VALVE, MIC NON-STERILE LATEX GLOVES, ADI STERILE GAUZE SPONGES and HEMO-BARRIER.

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