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Integrated Endoscopy, Inc.

United StatesFDA applicant, unverified FDA FEI 3011401113

Integrated Endoscopy, Inc. is a medical device manufacturer, with 10 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 14 Nov 2026.

Devices
10
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 7
  • FDA 510(k) 3

A device listed in two registries counts in both.

Device classes
  • FDA Class II 6
  • FDA Class I 4
Identifiers
  • FDA FEI 3011401113
  • DUNS 127632602

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Integrated Endoscopy, Inc. makes

Integrated Endoscopy, Inc. manufactures reusable arthroscopic access cannulas and rigid optical arthroscopes, including battery-powered models and wireless HD camera systems for arthroscopic procedures. Their portfolio includes reusable arthroscopes branded under the Nuvis series, designed for joint visualization in surgical settings.

The company’s devices are classified under FDA categories Class I and Class II, with regulatory records including 510(k) clearances and FDA’s Unique Device Identifier (UDI) listings.

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

Catalogue10

Newest first, rows 1-10 of 10

  • Nuvis IE58CAN-1

    Listed Registry: GUDID Class:I

  • Nuvis IE58TR

    Listed Registry: GUDID Class:I

  • Nuvis IE4030

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

  • Nuvis 140-4010-1

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

  • Nuvis IE58CAN-2

    Listed Registry: GUDID Class:I

  • Nuvis IE58OB

    Listed Registry: GUDID Class:I

  • Nuvis IE4030-10

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

  • Nuvis Battery Arthroscope Ref K191594

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

  • Nuvis Arthroscope Ref K140903

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

  • Nuvis® Wireless HD Camera System (Nuvis-2K) Ref K242606

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

Company details

FDA FEI number
3011401113
DUNS number
127632602
Address
16 Technology Drive, Suite 165, Irvine, CA, 92618
Website
iescope.com
Phone
17149552400

From the company website

Read 18 Oct 2026

Integrated Endoscopy is revolutionizing rigid endoscopes. nuvis Single-use Arthroscope delivers superior visualization and eliminates bioburden.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Integrated Endoscopy, Inc. have in the registry?

The registry currently lists 10 devices for Integrated Endoscopy, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Integrated Endoscopy, Inc.'s devices?

Among its 10 most recently registered devices, Integrated Endoscopy, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Integrated Endoscopy, Inc.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Integrated Endoscopy, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Integrated Endoscopy, Inc. in the registry?

The most recently registered devices listed for Integrated Endoscopy, Inc. include Nuvis IE58CAN-1, Nuvis IE58TR, Nuvis IE4030 and Nuvis 140-4010-1.

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