American Bantex Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What American Bantex Corp. makes
American Bantex Corp. manufactures mobility aids, including the MS 4 Mini Scooter and MS 3 model for patient transport, as well as medical-grade humidifiers (dry and bubble types) like the B9000 (3 PSI) and B9100 (6 PSI) for respiratory therapy. The company also produces the Tango BP1, a blood pressure monitoring device, and sterile surgical latex gloves (Type 1 natural rubber latex) for clinical use.
The portfolio includes devices classified under FDA Class I and Class II, with several models authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
American Bantex Ms 4 Mini Scooter Ref K040754
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
American Bantex, Model Ms 3 Ref K042104
Regimes: 510(k) Registry: 510(k)Tango, Models, BP1 Ref K031711
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Bantex Corp. have in the registry?
The registry currently lists 5 devices for American Bantex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Bantex Corp.'s devices?
Among its 5 most recently registered devices, American Bantex Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do American Bantex Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Bantex Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Bantex Corp. in the registry?
The most recently registered devices listed for American Bantex Corp. include AMERICAN BANTEX MS 4 MINI SCOOTER, AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSI, AMERICAN BANTEX, MODEL MS 3 and TANGO, MODELS, BP1.