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Axiom Medical, Inc.

United StatesFDA applicant, unverified FDA FEI 2020735

Devices
28
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Axiom Medical, Inc. makes

Axiom Medical, Inc. manufactures medical devices including silicone catheters for epistaxis and feeding, trocar catheters for minimally invasive procedures, wound drains (e.g., multipurpose and hydromer types), gastro sump drains, wound dressings, and fluid collection bags. Their portfolio also covers thoracic catheters, closed wound drains with trocars, and specialized wound management products like Lig-A-Boots.

The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue28

Newest first, rows 1-28 of 28

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  • Silicone Soft-Pak Epistaxis Catheter Ref K832476

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

  • Axiom Atraum Trocar Catheter Ref K852241

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

  • Axiom Feeding Gastro Tube Ref K831823

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

  • Catheter Thoracic, Axiom Ref K770983

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

  • Atraum Wound Dressing--Modification Ref K922760

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

  • Disposable Fluid Collection Bag Ref K904133

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

  • Glassman Silicone Catheter Ref K934895

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

  • Axiom Multipurpose Wound Drain Ref K993592

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

  • Axiom Hydromer Wound Drains Ref K832416

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

  • Axiom Gastro Sump Drain Ref K791509

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

  • Axiom Lig-A-Boots Ref K820161

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

  • Flat Closed Wound Drain With Trocar Ref K965146

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

  • Suction System Ref K904218

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

  • Suction System Ref K861306

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

  • Axiom Perfussion Cannula Ref K832475

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

  • Interpleural Anesthesia Catheter Ref K971851

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

  • Axiom Filtered Connector Ref K791508

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

  • Pvc Round Wound Drains Ref K905422

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

  • Auto-Clip Ref K771021

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

  • Axiom Vessel Loops Ref K800015

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

  • Tubing, Axiom Silicone Penrose Ref K781749

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

  • Catheter, Umbilicar Artery Ref K771022

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

  • Axiom Trocar Thoracic Catheter Ref K863247

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

  • Axiom Femoral Venus Catheter Ref K842084

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

  • Axiom Thoracic Catheters Ref K841593

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

  • Atraum Wound Dressing Ref K852614

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

  • Catheters, Drainage Ref K771048

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

  • Quazar Esophageal Stethoscope Ref K841574

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

Rows 1-28 of 28

Company details

FDA FEI number
2020735
Address
19320 SOUTH VAN NESS AVE., TORRANCE, CA, 90501

Frequently asked questions

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

The registry currently lists 28 devices for Axiom Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Axiom Medical, Inc.'s devices?

Among its 28 most recently registered devices, Axiom Medical, Inc. has devices listed in FDA 510(k) (28 devices).

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

Among its 28 most recently registered devices, the classes recorded for Axiom Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Axiom Medical, Inc. include SILICONE SOFT-PAK EPISTAXIS CATHETER, AXIOM ATRAUM TROCAR CATHETER, AXIOM FEEDING GASTRO TUBE and CATHETER THORACIC, AXIOM.

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