Medical Device Manufacturer · US , Sarasota , FL

Intertape Polymer Group

1 submissions · 1 cleared · Since 2026
1
Total
1
Cleared
0
Denied

Intertape Polymer Group — FDA 510(k) Submissions

Intertape Polymer Group has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Indicator, Physical/chemical Sterilization Process . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 General Hospital 1