Bryan Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What Bryan Corp. makes
Bryan Corp. makes hysteroscopes, tracheobronchial stents, laparoflators, and biotrace devices such as the BAGGISH hysteroscope, DUMON tracheobronchial stent, microprocessed controlled laparoflator, DUMON/HARRELL stent, and BIOTRACE Model 1730.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Baggish, Hysteroscope Ref K881249
510(k) 510(k)Dumon Tracheobronchial Stent Ref K894380
510(k) 510(k)Microprocessed Controlled Laparoflator Ref K913242
510(k) 510(k)Dumon/Harrell Ref K854414
510(k) 510(k)Biotrace, Model 1730 Ref K002063
510(k) 510(k)
Frequently asked questions
How many devices does Bryan Corp. have in the registry?
The registry currently lists 5 devices for Bryan Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bryan Corp.'s devices?
Among its 5 most recently registered devices, Bryan Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Bryan Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Bryan Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bryan Corp. in the registry?
The most recently registered devices listed for Bryan Corp. include BAGGISH, HYSTEROSCOPE, DUMON TRACHEOBRONCHIAL STENT, MICROPROCESSED CONTROLLED LAPAROFLATOR and DUMON/HARRELL.