Pacific Implant, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pacific Implant, Inc. makes
Pacific Implant, Inc. manufactures titanium endodontic points and intraosseous dental implants, designed for dental procedures requiring precise placement within bone or root canals.
These devices are classified as Class I and Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Pacific Implant Titanium Endodontic Point Ref K992582
Regimes: 510(k) Registry: 510(k)Intraosseous Dental Implant Ref K813227
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pacific Implant, Inc. have in the registry?
The registry currently lists 2 devices for Pacific Implant, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pacific Implant, Inc.'s devices?
Among its 2 most recently registered devices, Pacific Implant, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pacific Implant, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pacific Implant, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pacific Implant, Inc. in the registry?
The most recently registered devices listed for Pacific Implant, Inc. include PACIFIC IMPLANT TITANIUM ENDODONTIC POINT and INTRAOSSEOUS DENTAL IMPLANT.