Osteo Implant Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Osteo Implant Corp. makes
Osteo Implant Corp. manufactures titanium dental implants designed for osseointegration in oral and maxillofacial applications, as well as bone drills for surgical preparation in implant procedures. Their dental implants are intended for use in tooth replacement, while the bone drills assist in creating precise osteotomies during implant placement.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. These devices are intended for use within the United States, adhering to FDA compliance requirements for dental and surgical instrumentation.
Catalogue
Osteo Titanium Dental Implant Ref K862854
Regimes: 510(k) Registry: 510(k)Bone Drill Ref K945706
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteo Implant Corp. have in the registry?
The registry currently lists 2 devices for Osteo Implant Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteo Implant Corp.'s devices?
Among its 2 most recently registered devices, Osteo Implant Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Osteo Implant Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Osteo Implant Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteo Implant Corp. in the registry?
The most recently registered devices listed for Osteo Implant Corp. include OSTEO TITANIUM DENTAL IMPLANT and BONE DRILL.