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Ndm Corp.

United StatesFDA applicant, unverified

Devices
11

What Ndm Corp. makes

Ndm Corp. manufactures single-use electrosurgical devices, including disposable pens, grounding pads, and infant electrosurgical drapes, as well as wound dressings and adhesive tapes for medical procedures. Their portfolio also includes ECG monitoring accessories like adhesive electrodes, backpads, and paper tape electrodes, alongside peripheral nerve stimulation (PNS) electrodes and a skin abrading tool for procedural preparation. Intravenous catheters and a holster for electrosurgical pens are also part of their product line.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. These products are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue11

Newest first, rows 1-11 of 11

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  • Ndm Diatemp Infant Electrosurg. Disp. P. Ref K810920

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ndm Switchpen Holster Ref K901145

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Diatemp Electrosurgical Pen Ref K853968

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Clearsite Sterile Wound Dressing, Ndm Wound Dressi Ref K926202

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Electrosurgical Grounding Pad Ref K772160

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • I.V. Catheter Ref K772354

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • V-Trace Ecg Backpad Ref K761301

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ndm Paper Tape Ecg Electrode Ref K790730

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ndm Diatemp Electrosurgical Dis. Pad Ref K801158

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Electrode, Pns Ref K760312

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Pencil Skin Abrader Ref K830663

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

Rows 1-11 of 11

Frequently asked questions

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

The registry currently lists 11 devices for Ndm Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ndm Corp.'s devices?

Among its 11 most recently registered devices, Ndm Corp. has devices listed in FDA 510(k) (11 devices).

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

Among its 11 most recently registered devices, the classes recorded for Ndm Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Ndm Corp. include NDM DIATEMP INFANT ELECTROSURG. DISP. P., NDM SWITCHPEN HOLSTER, DIATEMP ELECTROSURGICAL PEN and CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI.

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