Skip to content

Intertape Polymer, 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 Intertape Polymer, Inc. makes

Intertape Polymer, Inc. manufactures Type 1 bismuth process indicator tapes designed for use in steam sterilization procedures. These tapes visually confirm exposure to sterilization conditions, ensuring proper processing of medical devices and equipment.

The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

FDA establishments1

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

  • Intertape Polymer Inc. Cornwall Ontario · CA FEI 3011494162

Frequently asked questions

How many devices does Intertape Polymer, Inc. have in the registry?

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

Which registries list Intertape Polymer, Inc.'s devices?

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

What risk classes do Intertape Polymer, Inc.'s devices fall under?

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

What are the newest devices from Intertape Polymer, Inc. in the registry?

The most recently registered devices listed for Intertape Polymer, Inc. include Intertape Polymer Inc., Type 1 Bismuth Process Indicator Steam Sterilization Tape.

Which FDA establishments are linked to Intertape Polymer, Inc.?

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

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