American Biosurgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 42
What American Biosurgical, Inc. makes
American Biosurgical, Inc. manufactures electrosurgical cables and cords, including bipolar and monopolar variants designed for surgical procedures. These devices are intended for use with electrosurgical units to facilitate tissue cutting, coagulation, and desiccation in operating room settings.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The manufacturer is based in the United States.
Catalogue
Search and filter all 42 devicesFrequently asked questions
How many devices does American Biosurgical, Inc. have in the registry?
The registry currently lists 42 devices for American Biosurgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Biosurgical, Inc.'s devices?
Among its 42 most recently registered devices, American Biosurgical, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (39 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do American Biosurgical, Inc.'s devices fall under?
Among its 42 most recently registered devices, the classes recorded for American Biosurgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Biosurgical, Inc. in the registry?
The most recently registered devices listed for American Biosurgical, Inc. include AMERICAN BIOSURGICAL AB 6005 A, AMERICAN BIOSURGICAL AB 1000(S), AMERICAN BIOSURGICAL AB 2001 B A and AMERICAN BIOSURGICAL AB 5003 (S).