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Dormer Laboratories, Inc.

Country not established FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Dormer Laboratories, Inc. makes

Dormer Laboratories, Inc. manufactures IQ Chambers, which are specialized containment systems designed for handling and processing infectious or hazardous biological materials in laboratory settings.

The company’s IQ Chambers are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The product portfolio is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Iq Chambers Ref K992553

    Class I
    Active 510(k) 510(k) I

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Dormer Laboratories, Inc. Toronto Ontario · CA FEI 3001344828

Frequently asked questions

How many devices does Dormer Laboratories, Inc. have in the registry?

The registry currently lists 1 device for Dormer Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dormer Laboratories, Inc.'s devices?

Among its 1 most recently registered device, Dormer Laboratories, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Dormer Laboratories, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Dormer Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Dormer Laboratories, Inc. in the registry?

The most recently registered devices listed for Dormer Laboratories, Inc. include IQ CHAMBERS.

Which FDA establishments are linked to Dormer Laboratories, Inc.?

1 FDA establishment is linked to Dormer Laboratories, Inc. in the registry; they are listed on the company page.

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