Bowen & Company, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 14
What Bowen & Company, Inc. makes
Bowen & Company, Inc. makes surgical instruments including cannulas, knot passers, power awls, arthroscopic rasps, shavers, electrodes, probes, suture drills, body graspers, suture passers, and skin preparatory cleansers.
The company's devices are classified as Class I, Class II, and unclassified (U) and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does Bowen & Company, Inc. have in the registry?
The registry currently lists 14 devices for Bowen & Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bowen & Company, Inc.'s devices?
Among its 14 most recently registered devices, Bowen & Company, Inc. has devices listed in FDA 510(k) (14 devices).
What risk classes do Bowen & Company, Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Bowen & Company, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bowen & Company, Inc. in the registry?
The most recently registered devices listed for Bowen & Company, Inc. include BOWEN CANNULA, BOWEN KNOT PASSER, STERNAL POWER AWL and MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP.