Ibt, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Ibt, Inc. makes
Ibt, Inc. manufactures the INTERSTRAND 125 and INTERSTRAND 103, including model numbers 1251S and 1031S, which are designed for medical imaging applications, specifically as interventional markers or guidewires for procedural guidance.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Ez-Pak (Ez-Pak Is A Trademark Of Ibt S.A.) Ref K041702
Regimes: 510(k) Registry: 510(k)Optistrand, Model 1032S Ref K043336
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ibt, Inc. have in the registry?
The registry currently lists 3 devices for Ibt, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ibt, Inc.'s devices?
Among its 3 most recently registered devices, Ibt, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ibt, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ibt, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ibt, Inc. in the registry?
The most recently registered devices listed for Ibt, Inc. include EZ-PAK (EZ-PAK IS A TRADEMARK OF IBT S.A.), OPTISTRAND, MODEL 1032S and INTERSTRAND 125 & INTERSTRAND 103, MODEL NUMBERS 1251S AND 1031S.