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Inrad

Also registered as Inrad, Inc.

Country not established

Inrad is a medical device manufacturer, with 138 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) and 1 FDA recall as of 13 Nov 2026.

Devices
138
FDA recalls
1

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 123
  • FDA 510(k) 15

A device listed in two registries counts in both.

Device classes
  • FDA Class II 86
  • FDA Class I 52
FDA recalls
Identifiers
  • DUNS 940023385

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Inrad makes

Inrad manufactures single-use biopsy tools, including side-notch biopsy gun handpieces and needles for soft-tissue sampling, as well as body aspiration needles. The company also produces non-vascular catheter introduction sets and intravenous fluid bag spikes for medical procedures.

These devices are regulated under FDA classifications, with most falling into Class I or Class II. They are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries, reflecting their compliance with U.S. medical device regulations.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue138

Newest first, rows 1-50 of 138

Search and filter all 138 devices
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  • Inrad 53220

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

  • Inrad 53222

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

  • Inrad 53218

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

  • Inrad 41222

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

  • Inrad 41218

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

  • Inrad 41220

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

  • Inrad 41820

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

  • Inrad 41822

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

  • Inrad 45018

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

  • Inrad 45118

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

  • Inrad 45222

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

  • Inrad 45020

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

  • Inrad 45120

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

  • Inrad 45122

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

  • Inrad 45022

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

  • Inrad 54018

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

  • Inrad 54118

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

  • Inrad 54120

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

  • Inrad 54222

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

  • Inrad 54122

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

  • Inrad 54020

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

  • Inrad 42118

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

  • Inrad 54022

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

  • Inrad 42120

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

  • Inrad 42020

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

  • Inrad 42122

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

  • Inrad 44022

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

  • Inrad 44020

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

  • Inrad 54501

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

  • Inrad 15423

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

  • Inrad 15425

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

  • Inrad 54818

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

  • Inrad 54820

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

  • Inrad 54822

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

  • Inrad 54720

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

  • Inrad 54722

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

  • Inrad 54922

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

  • Inrad 53722

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

  • Inrad 53922

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

  • Inrad 53822

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

  • Inrad 53820

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

  • Inrad 53720

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

  • Inrad 53818

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

  • Inrad 620916

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

  • Inrad 620918

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

  • Inrad 620920

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

  • Inrad 621516

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

  • Inrad 621518

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

  • Inrad 621520

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

  • Inrad 640914

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

Rows 1-50 of 138

Showing 1-50 of 138

Company details

DUNS number
940023385
Phone
6163017800

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by Inrad, initiated on 2010-12-20. By recorded status: 1 terminated. The reasons filed fall into these groups: labeling or instructions for use, packaging and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2010

    • 20 Dec 2010 Z-1063-2011 Unclassified (pre-2012) Terminated This lot of product has the wrong expiration date on the carton label. The pouches contained the correct expiration date. Distribution: Nationwide Distribution: USA including states of: FL, GA, KY, NH, NJ, NM, PA , SC, WA, and WI. Submission number: K813368

Frequently asked questions

How many devices does Inrad have in the registry?

The registry currently lists 138 devices for Inrad. Devices recorded under merged duplicate company entries are counted once.

Which registries list Inrad's devices?

Among its 50 most recently registered devices, Inrad has devices listed in FDA GUDID (50 devices).

What risk classes do Inrad's devices fall under?

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

Are there FDA recall records for Inrad?

FDA recall records list 1 recall initiated by Inrad, the most recent initiated on 20 Dec 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Inrad in the registry?

The most recently registered devices listed for Inrad include Inrad 53220, Inrad 53222, Inrad 53218 and Inrad 41222.

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