Data / Medical devices / Canada / Intertape Polymer Inc.
Intertape Polymer Inc.: FDA-registered device maker in Cornwall Ontario, Canada, 3 510(k) clearances
Intertape Polymer Inc. is registered with the FDA (registration 3011494162) in Cornwall Ontario, Canada. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated August 2, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011494162
- Address
- 1400 Rosemount Ave, Cornwall Ontario, Canada, K6J 3E6
- Owner or operator
- Intertape Polymer Corp. (10047882)
- Roles
- Manufacturer
- First device listed
- November 12, 2014
- Registered through
- 2026
- Brand names listed
- Indicator Tape
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Indicator, Physical/Chemical Sterilization Process | JOJ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 2, 2019 | K191741 | Intertape Polymer Inc., Type 1 Bismuth Process Indicator Steam Sterilization Tape | JOJ | Substantially Equivalent | Intertape Polymer, Inc. | accessdata.fda.gov |
| June 28, 2016 | K161024 | Canadian Technical Tape, LTd. LF Process Indicator Steam Sterilization Tape | JOJ | Substantially Equivalent | Canadian Technical Tape, Ltd. | accessdata.fda.gov |
| October 27, 2014 | K140940 | PROCESS INDICATOR TAPE FOR STEAM STERILIZATION | JOJ | Substantially Equivalent | Canadian Technical Tape, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 2, 2019. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.