Bud Industries, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Bud Industries, Inc. makes
Bud Industries, Inc. manufactures dental and maxillofacial implant systems, including titanium-based implants for dental reconstruction and bone integration. Their portfolio includes specific implant lengths, such as 4.0mm and 5.5mm variants, designed for oral and facial surgical applications.
The company’s implants are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. Their products are listed in the FDA’s 510(k) database, adhering to U.S. regulatory requirements for surgical implants.
Catalogue
Bud Dental Implant System Ref K902331
510(k) 510(k)Bud Maxillofacial Implant System Ref K913688
510(k) 510(k)Dental Implant System 4.0mm And 5.5mm Length Ref K912521
510(k) 510(k)
Frequently asked questions
How many devices does Bud Industries, Inc. have in the registry?
The registry currently lists 3 devices for Bud Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bud Industries, Inc.'s devices?
Among its 3 most recently registered devices, Bud Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bud Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bud Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bud Industries, Inc. in the registry?
The most recently registered devices listed for Bud Industries, Inc. include BUD DENTAL IMPLANT SYSTEM, BUD MAXILLOFACIAL IMPLANT SYSTEM and DENTAL IMPLANT SYSTEM 4.0MM AND 5.5MM LENGTH.